Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → 3'-Chloro-4'-fluoroacetophenone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Acetyl chloride | HCID 6367 | — |
| 반응물 | 1-Chloro-2-fluorobenzene | HCID 9583 | — |
| 반응물 | 3-Chloro-4-fluorobenzoyl Chloride | HCID 2736548 | — |
| 반응물 | Aluminum(III) Chloride | HCID 6451240 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Carbon Disulfide | HCID 6348 | — |
| 용매 | Tetrachloroethylene | HCID 31373 | — |
| 생성물 | 3'-Chloro-4'-fluoroacetophenone | HCID 520422 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06187952B1 |
| 출처 데이터셋 | uspto-grants-2001_02 |
| ORD ID | ord-f9495f7508b342e992643886567fff12 |
| 출처 메모 | uspto-grants-2001_02 |