Epibromohydrin → 3-Isopropyl-5-[2-(2,3-epoxypropoxy)-styryl]-isoxazole
반응식
[H-].[Na+].[CH:3]([C:6]1[CH:10]=[C:9]([CH:11]=[CH:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[OH:19])[O:8][N:7]=1)([CH3:5])[CH3:4].[CH2:20]([CH:22]1[O:24][CH2:23]1)Br>>[CH:3]([C:6]1[CH:10]=[C:9]([CH:11]=[CH:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[O:19][CH2:20][CH:22]2[O:24][CH2:23]2)[O:8][N:7]=1)([CH3:5])[CH3:4]참가 물질
4
실험 절차
This is prepared, using the method described in Example VI, from 3.4 g of 55% strength sodium hydride (0.078 mole), 18 g (0.078 mole) of 3-isopropyl-5-(2-hydroxystyryl)-isoxazole and 10.8 g (0.078 mole) of epibromohydrin. 21.5 g (97% of theory) of a colorless oil are obtained.
후처리
- customThis is prepared
- custom21.5 g (97% of theory) of a colorless oil are obtained
출처 및 근거
- ORD 기록
- ord-beada3a2000943d893332687dbbc29c0
- 출처 데이터셋
- uspto-grants-1981_12
- 특허 번호
- US04305951
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