反応式
[C:1]([C:5](=[CH:10][C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[CH:12]=1)[CH2:6][C:7]([OH:9])=[O:8])([O:3][CH3:4])=[O:2]>C(O)(=O)C.[Pd]>[C:1]([CH:5]([CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[CH:12]=1)[CH2:6][C:7]([OH:9])=[O:8])([O:3][CH3:4])=[O:2]参加物
4
実験手順
A solution of 21.1 g (84 mmol) of 3-carbomethoxy-4-(3-methoxyphenyl)-3-butenoic acid in 100 ml of acetic acid with 2.11 g of 10% Pd on carbon is shaken under H2 atmosphere until H2 uptake ceases (approximately 4 hours). This is filtered through celite and the filtrate concentrated in vacuo several times from toluene to afford 17.6 g of 3-carbomethoxy-4-(3-methoxyphenyl)butanoic acid in the form of a yellow oil which is used directly in the next step.
後処理
- filtrationThis is filtered through celite
- concentrationthe filtrate concentrated in vacuo several times from toluene
出典と根拠
- ORDレコード
- ord-a131f54ab91a46f0a140d8f163f67720
- 出典データセット
- uspto-grants-1995_11
- 特許番号
- US05468898
関連ノート
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