Acetyl chloride → HCID 66909120, 화합물
반응식
[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[O:11][C:12]([F:15])([F:14])[F:13].[C:16](Cl)(=O)C>CO>[CH3:16][O:7][C:6](=[O:8])[C:5]1[CH:9]=[CH:10][C:2]([F:1])=[C:3]([O:11][C:12]([F:14])([F:13])[F:15])[CH:4]=1참가 물질
4
실험 절차
To a stirred suspension of 21.2 g (96.9 mmol) 4-Fluoro-3-trifluoromethoxy-benzoic acid (JRD-Fluoro) and 161 ml methanol were added 30.4 g (387.6 mmol) acetyl chloride drop wisely at 0° C. The reaction mixture was stirred over night, filtered and concentrated. The residue was diluted with dichloromethane, washed with diluted sodium hydrogen carbonate solution, dried with sodium sulphate and concentrated. The residue was purified by column chromatography (hexane:ethylacetate). The desired product 14a was obtained in 75% yield (17.3 g; 72.7 mmol)
후처리
- customdrop wisely at 0° C
- filtrationfiltered
- concentrationconcentrated
- additionThe residue was diluted with dichloromethane
- washwashed with diluted sodium hydrogen carbonate solution
- dry with materialdried with sodium sulphate
- concentrationconcentrated
- customThe residue was purified by column chromatography (hexane:ethylacetate)
출처 및 근거
- ORD 기록
- ord-053d53668dbd4344b507744711ca611e
- 출처 데이터셋
- uspto-grants-2013_10
- 특허 번호
- US08557776B2
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