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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1980226생성일: 2026년 10월 26일

Hydrochloric Acid → alpha-Cyano-phenylacetic acid pentachlorophenylester

https://huagongshe.com/reaction/1980226

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PentachlorophenolHCID 992—
반응물PyridineHCID 1049—
반응물Phosphorus pentachlorideHCID 24819—
반응물alpha-Cyanobenzeneacetic acidHCID 26403—
용매Carbon TetrachlorideHCID 5943—
용매DichloromethaneHCID 6344—
생성물alpha-Cyano-phenylacetic acid pentachlorophenylesterHCID 20402417—

반응 단계

8 g. (0.05 moles) of α-cyano-phenylacetic acid are dissolved in 80 ml. of dichloromethane, 10.2 g. (0.05 moles) of phosphorous pentachloride are added and the mixture is stirred for 2 hours at the boiling point of the dichloromethane. The reaction is completed when the hydrochloric acid evolution ceases. The solvent is distilled off and the residue containing the obtained acid chloride and phosphoroxychloride is taken up in carbontetrachloride and the solution is added dropwise to 13 g. (0.05 moles) of pentachlorophenol and 4 ml. (0.05 moles) of pyridine dissolved in 200 ml. of carbontetrachloride. The reaction mixture is cooled and the precipitated pyridine chlorohydrate is removed by washing twice with 50 ml. of water, dried, distilled off and the residue is distilled off with diisopropyl ether. The precipitated crystalline product is cooled and filtered. The α-cyanophenylacetic acid pentachlorophenyl ester is air-dried.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04508658
출처 데이터셋uspto-grants-1985_04
ORD IDord-43ffbc2a2594471d80d70c227c2d8036
출처 메모uspto-grants-1985_04