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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64978생성일: 2026년 10월 23일

Hydrochloric Acid → 2,2-Dichlorovinyl 2,4-dichloro-5-fluorophenyl ketone

https://huagongshe.com/ko/reaction/64978

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Vinylidene chlorideHCID 6366—
반응물2,4-Dichloro-5-fluorobenzoyl chlorideHCID 2736821—
반응물Aluminum(III) ChlorideHCID 6451240—
용매DichloromethaneHCID 6344—
생성물2,2-Dichlorovinyl 2,4-dichloro-5-fluorophenyl ketoneHCID 1364500696.7%

반응 단계

136.5 g (0.6 mole) of 2,4-dichloro-5-fluorobenzoyl chloride and 97 g (1 mole) of 1,1-dichloroethylene are successively added dropwise to a suspension of 84 g of anhydrous aluminum chloride in 300 ml of methylene chloride, while cooling with ice and stirring, during which the temperature should not exceed 30° C. The mixture is stirred at room temperature for 3 hours and poured onto a mixture of about 600 g of ice and 60 ml of concentrated hydrochloric acid, the organic phase is separated off and the aqueous phase is subsequently extracted three times with 100 ml of methylene chloride. The methylene chloride solution is washed with 100 ml of water and dried with sodium sulphate and the solvent is distilled off in vacuo. The residue (218.8 g) is heated at 130°-140° C. with 0.34 g of triphenylphosphine until the initially vigorous evolution of HCl has ended (about 3/4 hour). Distillation under a fine vacuum gives 167.1 g (96.4%) of 2,2-dichlorovinyl 2,4-dichloro-5-fluorophenyl ketone of boiling point 121°-123° C./0.13 mbar, melting point 64°-65° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04611080
출처 데이터셋uspto-grants-1986_09
ORD IDord-03763ae0925344f3812ce949ad967c38
출처 메모uspto-grants-1986_09