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Relevant bibliographies by topics / Chloroacetyl chloride

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Academic literature on the topic 'Chloroacetyl chloride'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Chloroacetyl chloride"

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D’Souza, Malcolm J., Zoon Ha Ryu, Byoung-Chun Park та Dennis N. Kevill. "Correlation of the rates of solvolysis of acetyl chloride and α-substituted derivatives". Canadian Journal of Chemistry 86, № 5 (2008): 359–67. http://dx.doi.org/10.1139/v08-028.

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Additional specific rates of solvolysis have been determined for acetyl chloride and diphenylacetyl chloride. These are combined with literature values to carry out correlation analyses, using the extended Grunwald–Winstein equation with incorporation of literature values for solvent nucleophilicity (NT) and solvent ionizing power (YCl). Parallel analysis are carried out using literature values for the specific rates of solvolysis of trimethylacetyl chloride, chloroacetyl chloride, phenylacetyl chloride, and α-methoxy-α-trifluoromethylphenylacetyl chloride (MTPAC). Chloroacetyl chloride and MT

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2

Zhao, Hong Chi, Juan Li Guo, Ai Juan Sun, and Ling Ling Gao. "Synthesis and Properties of Linear Chloroacetylated Polystyrene." Key Engineering Materials 428-429 (January 2010): 102–5. http://dx.doi.org/10.4028/www.scientific.net/kem.428-429.102.

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Polystyrene (PS) was synthesized by emulsion polymerization. The linear chloroacetylated PS was prepared high effectively by Friedel-Crafts acetylation of PS using chloroacetyl chloride and anhydrous aluminium chloride as chloroacetylation reagent and catalysts, respectively. The structure of chloroacetyl group is similar to that of chloromethyl group. In this method, carcinogenic compound (chloromethyl ether etc.) was avoided and the reactions of secondary cross link and multi-substitute could be eliminated. The resultant polymers were characterized by Fourier transform infrared spectrometery

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3

Journal, Baghdad Science. "Synthesis of Some new 2-(4-Aryliminophenoxy)N-Arylacetamide Via p-hydroxy benzaldehyde." Baghdad Science Journal 11, no. 2 (2014): 486–90. http://dx.doi.org/10.21123/bsj.11.2.486-490.

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Chloroacetamide derivatives (2a-g) have been prepared through reaction of chloroacetyl chloride(1) (which prepared by the reaction of chloroacetic acid with thionyl chloride) with primary aromatic amines and sulfa compounds to afford compounds (2a-g) which then reacted with p-hydroxy benzaldehyde via Williamson reaction to obtaine the new compounds 2-(4-formyl phenoxy)-N-aryl acetamide (3a-g). Finally , compounds (3a-g) will be use as a good synthon to prepare the Schiff bases represented by compounds 2-(4-aryliminophenoxy)-N-arylacetamide (4a-g). through , reaction with some primary aromatic

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4

Sakarya, Handan Can, and Aslı Ketrez. "Synthesis of Novel cis-2-Azetidinones from Imines and Chloroacetyl Chloride Using Triethylamine." Acta Chimica Slovenica 70, no. 4 (2023): 628–33. http://dx.doi.org/10.17344/acsi.2023.8451.

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A synthesis of a novel series of cis-2-azetidinones 2a–c was carried out by the cycloaddition reaction of imine 1a–c and chloroacetyl chloride in dry dichloromethane at 0–5 °C using triethylamine. The cycloaddition of the Schiff bases with chloroacetyl chloride resulted in the corresponding major product cis-2-azetidinone stereoisomers 2a–c. The synthesized compounds were characterized by analytical and spectral techniques (infrared, 1H NMR, 13C NMR, and elemental analysis).

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5

Tolba, Mahmoud S., Mostafa Sayed, Shaban A. A. Abdel-Raheem, Taher A. Gaber, Adel M. Kamal El-Dean, and Mostafa Ahmed. "Synthesis and spectral characterization of some new thiazolopyrimidine derivatives." Current Chemistry Letters 10, no. 4 (2021): 471–78. http://dx.doi.org/10.5267/j.ccl.2021.4.004.

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Thiazolopyrimidnes are considered one of the most interesting classes in heterocyclic chemistry due to their pharmaceutical importance. Herein, we report the synthesis of some new heterocyclic compounds containing thiazolopyrimidine starting from compound (1) which was previously prepared in literature. The starting compound was allowed to react with different alkylating agents such as chloroacetone, chloroacetyl chloride, and phenacyl bromide to afford derivatives (2-4). Compound (5), benzylidene derivative, was obtained by the reaction of compound (2) with benzaldehyde while amino-dicarbonit

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6

Goodall, Karen, та Andrew F. Parsons. "The Synthesis of α, β–Dehydroamino Acid Esters from Hydroxyamino Esters using Haloacetyl Halides". Journal of Chemical Research 2000, № 2 (2000): 54–55. http://dx.doi.org/10.3184/030823400103166508.

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The preparation of dehydroamino acid esters from reaction of β–hydroxy–α–amino esters with dichloroacetyl chloride, chloroacetyl chloride or trichloroacetyl chloride in the presence of base has been investigated.

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7

Al-muamin, Thanaa, Naeemah Al-lami, Suroor Rahman, and Rana Ali. "Synthesis, Characterization and Antimicrobial Activity of New Nucleoside Analogues from Benzotriazole." Chemistry & Chemical Technology 10, no. 3 (2016): 271–78. http://dx.doi.org/10.23939/chcht10.03.271.

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Novel derivatives of 1-(´1, ´3, ´4, ´6-tetra benzoyl-β-D-fructofuranosyl)-1H- benzotriazole and 1-(´1, ´3, ´4, ´6-tetra benzoyl-β-D-fructofuranosyl)-1H-benzotriazole carrying Schiff bases moiety were synthesised and fully characterised. The protection of D-fructose using benzoyl chloride was synthesized, followed by nucleophilic addition/elimination between benzotriazole and chloroacetyl chloride to give 1-(1- chloroacetyl)-1H-benzotriazole. The next step was condensation reaction of protected fructose and 1-(1-chloroacetyl)-1H-benzotriazole producing a new nucleoside analogue. The novel nucle

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8

KRISHNA, C. JOSHI, N. PATHAK VIJAI, and K. GOYAL MAHENDRA. "Synthesis, Anticonvulsant and Analgesic Activities of some New Fluorine containing 1,3,5-Trisubstituted-hydantoins." Journal of Indian Chemical Society Vol. 62, Nov 1985 (1985): 904–8. https://doi.org/10.5281/zenodo.6325270.

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Department of Chemistry, University of Rajasthan Jaipur-302 004 Fifteen new fluorine containing Mannich bases derived from 1,5-disubstituted-arylhydantoins have been synthesised by treating the appropriate 1,5-disubstituted-arylhydantoins with secondary amine and formaldehyde in ethanol. Seven 1,5-disubstituted-arylhydantoins were treated with chloroacetyl chloride and the resulting 3chloroacetyl-derivatives converted into the corresponding 3-dialkylaminoacetyl-1,5- disubstituted-arylhydantoins on treatment with secondary amines. Representative compounds have been screened

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9

Furukawa, Mitsuru, Shigeru Kabashima, Yasuhiro Tomita, Tadashi Ohkawara, and Tetsuo Yamasaki. "Heterocyclizations of Thiosemicarbazones with a-Chloroacetyl Chloride." HETEROCYCLES 31, no. 12 (1990): 2139. http://dx.doi.org/10.3987/com-90-5541.

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Agirbag, Hikmet, Dogan Sümengen, Yaşar Dürüst, and Nedime Dürüst. "The Reaction of Amidoximes with Chloroacetyl Chloride." Synthetic Communications 22, no. 2 (1992): 209–17. http://dx.doi.org/10.1080/00397919208021295.

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Book chapters on the topic "Chloroacetyl chloride"

1

"Chloroacetyl chloride." In Toxicological Evaluations. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-60278-8_8.

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Dell, C. P. "Two Steps Using Chloroacetyl Chloride." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00051.

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Pfeiffer, W. D. "Reaction with Trichloroacetyl Chloride, Chloroacetyl Chloride, Benzoyl Chloride, or Ethyl Chloroformate." In Chlorine, Bromine, and Iodine. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-035-00161.

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Tidwell, T. T. "Chloroketene by Pyrolytic Dehydrochlorination of Chloroacetyl Chloride." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00099.

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Shimada, K. "Reaction of ,-Dialkyl-′-[(dimethylamino)methylene]selenoureas with Chloroacetyl Chloride." In Science of Synthesis Knowledge Updates KU 2010/4. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-111-00076.

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Kaur, Navjeet. "Synthesis of azetidines by cycloaddition of imines to chloroacetyl chloride-II." In Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023. http://dx.doi.org/10.1016/b978-0-443-19204-3.00006-1.

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Kaur, Navjeet. "Synthesis of azetidines by cycloaddition of imines to chloroacetyl chloride-I." In Synthesis of Azetidines from Imines by Cycloaddition Reactions. Elsevier, 2023. http://dx.doi.org/10.1016/b978-0-443-19204-3.00013-9.

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Conference papers on the topic "Chloroacetyl chloride"

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Dinh Thanh, Nguyen, Do Son Hai, Cao Thi Le, Vu Thi Tuyet Thuy, and Do Tien Tung. "SYNTHESIS OF 2-AMINO-4H-PYRAN-3-CARBONITRILES ITS REACTION WITH CHLOROACETYL CHLORIDE." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04770.

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Reports on the topic "Chloroacetyl chloride"

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Immediately dangerous to life or health (IDLH) value profile: chloroacetyl chloride (CAS no.79-04-9). U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 2016. http://dx.doi.org/10.26616/nioshpub2016169.

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