반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])=[CH:4][CH:3]=1.[C:13](Cl)(=O)C>CO>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][C:10]([O:12][CH3:13])=[O:11])=[CH:6][CH:7]=1참가 물질
4
실험 절차
To a stirred solution of 3-(4-chlorophenyl)propanoic acid (commercially available from Maybridge) (14.5 g, 77.1 mmol) in methanol (400 ml) was added acetyl chloride (50 ml) and the reaction mixture was refluxed for 20 h. After this time the reaction mixture was left to cool before being concentrated under reduced pressure. The residue was then dissolved in DCM (200 ml) and washed with 1M sodium hydroxide solution (100 ml). The organic layer was dried with magnesium sulphate and concentrated in vacuo to give the title product as a brown oil (15.7 g, 77 mmol, 100%); 1HNMR (400 MHz, CDCl3) δ: 2.55 (t, 2H), 2.9 (t, 2H), 3.6 (s, 3H), 7.1 (d, 2H), 7.2 (d, 2H).
후처리
- temperaturethe reaction mixture was refluxed for 20 h
- waitAfter this time the reaction mixture was left
- temperatureto cool
- concentrationbefore being concentrated under reduced pressure
- dissolutionThe residue was then dissolved in DCM (200 ml)
- washwashed with 1M sodium hydroxide solution (100 ml)
- dry with materialThe organic layer was dried with magnesium sulphate
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-6221743a92d34bf18a45f9ca94f86380
- 출처 데이터셋
- uspto-grants-2005_02
- 특허 번호
- US06849649B2
연결된 노트
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