反応式
[C:1]1([CH:7]([OH:11])[CH2:8][CH2:9][OH:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1([C@@H](O)CCO)C=CC=CC=1>CCCCCC.CC(O)C>[C:1]1([C:7](=[O:11])[CH2:8][CH2:9][OH:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
4
実験手順
Determination of the absolute configuration, optical purity and reaction yield of 1-phenyl-1,3-propanediol or a derivative thereof in the examples was determined by high pressure liquid chromatography (column: Chiral Cell OB, manufactured by Daisel Chemical Co., eluent: hexane/2-propanol (8/2), flow rate: 0.7 ml/min, detection: UV 210 nm). The reaction yield represents the mole percentage of (S)-1-phenyl-1,3-propanediol produced per mole of 1-phenylpropan-3-ol-1-one added as starting material.
後処理
- customThe reaction yield
出典と根拠
- ORDレコード
- ord-4ea4684372744d47a2f4a72e51f79258
- 出典データセット
- uspto-grants-1995_02
- 特許番号
- US05393664
関連ノート
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