반응식
Cl[CH2:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11](=[O:13])[CH3:12])=[CH:7][CH:6]=1.[C:14]([NH2:18])([CH3:17])([CH3:16])[CH3:15]>O>[CH3:15][C:14]([NH:18][CH2:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11](=[O:13])[CH3:12])=[CH:7][CH:6]=1)([CH3:17])[CH3:16]참가 물질
4
반응 조건
- 온도
- 120 °C
실험 절차
A mixture of 6.5 g of the product of Step A in 30 ml of tert.-butylamine was heated at 120° C. for 30 hours and was then diluted with water and extracted with ethyl acetate. The organic phase was washed with water, dried over a deshydrant, filtered and evaporated to dryness. The residue was chromatographed over silica and eluted with a 9-1 ethyl acetate-triethylamine mixture to obtain 7.264 g of 1-[4-{-2-(1,1-dimethylethylamino)-ethoxy}-phenyl]-ethanone.
후처리
- extractionextracted with ethyl acetate
- washThe organic phase was washed with water
- customdried over a deshydrant
- filtrationfiltered
- customevaporated to dryness
- customThe residue was chromatographed over silica
- washeluted with a 9-1 ethyl acetate-triethylamine mixture
출처 및 근거
- ORD 기록
- ord-fca304eb29c24e84bbfaa78ddfa3439e
- 출처 데이터셋
- uspto-grants-1989_08
- 특허 번호
- US04853408
연결된 노트
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