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[CH:1]([CH:3]([C:6]1[C:11]([CH3:12])=[CH:10][C:9]([CH3:13])=[CH:8][C:7]=1[CH3:14])[C:4]#[N:5])=O.Cl.[CH2:16]([O:18][C:19](=[O:23])[CH2:20][NH:21][CH3:22])[CH3:17]>C1C=CC=CC=1>[CH2:16]([O:18][C:19](=[O:23])[CH2:20][N:21]([CH3:22])[CH:1]=[C:3]([C:6]1[C:11]([CH3:12])=[CH:10][C:9]([CH3:13])=[CH:8][C:7]=1[CH3:14])[C:4]#[N:5])[CH3:17]참가 물질
4
실험 절차
A mixture of a-formyl-2,4,6 trimethylphenylacetonitrile (4.5 g, 24 mmol) and sarcosine ethyl ester hydrochloride (3.7 g, 24 mmol) in 100 mL of benzene was refluxed in a Dean-Stark apparatus for 16 h. The solvent was removed in vacuo to afford N-Methyl-N-[2-(2,4,6-trimethylphenyl)-2-cyanovinyl]-glycine ethyl ester as a pale yellow oil.
후처리
- temperaturewas refluxed in a Dean-Stark apparatus for 16 h
- customThe solvent was removed in vacuo
출처 및 근거
- ORD 기록
- ord-5e47cd794cfa43fabfef38e67bdb4b46
- 출처 데이터셋
- uspto-grants-1997_07
- 특허 번호
- US05644057
연결된 노트
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