반응식
[F:1][C:2]1[CH:12]=[CH:11][C:5]([C:6]([CH2:8][C:9]#[N:10])=[O:7])=[CH:4][CH:3]=1.[CH3:13][O:14][C:15](OC)(OC)[CH2:16][CH3:17].C(OC(=O)C)(=O)C>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([C:8](=[C:15]([O:14][CH3:13])[CH2:16][CH3:17])[C:9]#[N:10])=[O:7])=[CH:11][CH:12]=1참가 물질
4
실험 절차
A solution containing 30 g. of (p-fluorobenzoyl)acetonitrile, 36.4 g. of trimethylorthopropionate and 57 g. of acetic anhydride is heated in an oil bath at 130° for 3 hours. The ethanol and excess acetic anhydride is distilled off and the residue is diluted with chloroform. The chloroform solution is passed quickly through Magnesol® and concentrated, then cooled to produce the title product.
후처리
- additionA solution containing 30 g
- distillationThe ethanol and excess acetic anhydride is distilled off
- additionthe residue is diluted with chloroform
- concentrationconcentrated
- temperaturecooled
출처 및 근거
- ORD 기록
- ord-2829d8a5983b42ecacf78f16a0bc6537
- 출처 데이터셋
- uspto-grants-1979_11
- 특허 번호
- US04173650
연결된 노트
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