反応式
[C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10](=[O:12])[CH3:11])[CH:5]=1)(=[O:3])[CH3:2].[BH4-].[Na+]>>[CH3:11][CH:10]([C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([CH:1]([CH3:2])[OH:3])[CH:5]=1)[OH:12]参加物
3
実験手順
This mixture of stereoisomers was prepared from 1,3-diacetylbenzene by reduction with sodium borohydride as described above for the para stereoisomers. The mixture of stereoisomers was isolated as a semisolid. It appeared as a single spot on TLC and as a single peak on VPC.
後処理
- additionThis mixture of stereoisomers
- additionThe mixture of stereoisomers
- customwas isolated as a semisolid
出典と根拠
- ORDレコード
- ord-546ecb5962634cd395c40460dcb9740d
- 出典データセット
- uspto-grants-1992_11
- 特許番号
- US05166062
関連ノート
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