3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid → Methyl 4-hydroxy-3-methoxy-cinnamate

HRID 1249957

反応式

HRID 1249957 の反応式
[OH:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH:7][C:8]([OH:10])=[O:9])=[CH:4][C:3]=1[O:13][CH3:14].S(=O)(=O)(O)O.[CH3:20]O>>[OH:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH:7][C:8]([O:10][CH3:20])=[O:9])=[CH:4][C:3]=1[O:13][CH3:14]

参加物

4

実験手順

The preparation was effected analogously to Example 1 from 25 g (0.129 mol) of 4-hydroxy-3-methoxy-cinnamic acid and 180 ml of methanol with concentrated sulphuric acid as the catalyst. For purification, it was chromatographed on silica gel with dichloromethane/diethyl ether (19:1). This gave 21.78 g of methyl 4-hydroxy-3-methoxy-cinnamate as a pale yellow oil.

後処理

  1. customFor purification, it
  2. customwas chromatographed on silica gel with dichloromethane/diethyl ether (19:1)

出典と根拠

ORDレコード
ord-ecfe1b6085494f07b93e938c2ed914c2
出典データセット
uspto-grants-2002_01
特許番号
US06335409B1

関連ノート

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