Vinyl valerate → 4-(Tetrahydropyran-2-yloxy)phenylethanol
反応式
C([O:6][CH:7]([C:9]1[CH:14]=[CH:13][C:12]([O:15][CH:16]([O:18][CH2:19][CH3:20])[CH3:17])=[CH:11][CH:10]=1)[CH3:8])(=O)CCC.[C:21]([O:27][CH:28]=[CH2:29])(=[O:26])[CH2:22][CH2:23][CH2:24][CH3:25]>>[O:18]1[CH2:19][CH2:20][CH2:21][CH2:17][CH:16]1[O:15][C:12]1[CH:11]=[CH:10][C:9]([CH:7]([OH:6])[CH3:8])=[CH:14][CH:13]=1.[C:21]([O:27][CH2:28][CH3:29])(=[O:26])[CH2:22][CH2:23][CH2:24][CH3:25]参加物
4
実験手順
The procedure of Example 5 (i) was repeated except that vinyl valerate was used instead of 2,2,2-trichloroethyl butyrate to give 10.4 g of S-form of 1-(4-(tetrahydro-2-pyranyloxy)phenyl)ethanol (yield: 94%) and 13.9 g of R-form of 1-(4-tetrahydro-2-pyranyloxy)phenyl)ethyl valerate (yield: 91%).
出典と根拠
- ORDレコード