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HRID 635542생성일: 2026년 10월 26일

Hydrochloric Acid → 3'-Chloro-4'-fluoroacetophenone

https://huagongshe.com/reaction/635542

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Acetyl chlorideHCID 6367—
반응물1-Chloro-2-fluorobenzeneHCID 9583—
반응물3-Chloro-4-fluorobenzoyl ChlorideHCID 2736548—
반응물Aluminum(III) ChlorideHCID 6451240—
용매DichloromethaneHCID 6344—
용매Carbon DisulfideHCID 6348—
용매TetrachloroethyleneHCID 31373—
생성물3'-Chloro-4'-fluoroacetophenoneHCID 52042280%

반응 단계

3-Chloro-4-fluorobenzoyl chloride is available via a multi-stage synthesis. According to Diep et al., J. Chem. Soc. [1963], 2784-2787, ortho-chlorofluorobenzene is initially reacted with acetyl chloride in the presence of large amounts of aluminum chloride in the presence of carbon disulfide, methylene chloride or tetrachloroethylene, the reaction mixture is decomposed with dilute hydrochloric acid, the organic phase is washed with aqueous sodium hydroxide, then with water, and dried over sodium sulfate, the solvent is evaporated, and the residue is subjected to fractional distillation at reduced pressure. This method gives 3-chloro-4-fluoroacetophenone in a yield of about 80%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06187952B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-f9495f7508b342e992643886567fff12
출처 메모uspto-grants-2001_02