反応式
C[O:2][C:3](=[O:18])[CH:4]=[CH:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:8][CH:7]=1.[OH-].[K+]>C1COCC1.CO>[C:9]1([C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:10]=[CH:11][C:6]([CH:5]=[CH:4][C:3]([OH:18])=[O:2])=[CH:7][CH:8]=1参加物
実験手順
To a suspension of 3-biphenyl-4-yl-acrylic acid methyl ester (9.384 g, 39.38 mmol) in THF (120 ml) and MeOH (80 ml) was added 1N KOH (79 ml) and the mixture refluxed. After 3 h, heating was stopped. The reaction mixture was concentrated to about 50 ml, diluted with water (200 ml) and acidified with 2N HCl (80 ml). EtOAc (1000 ml) was added and the whole mixture heated to boiling to dissolve all solids. After cooling, the layers were separated and the organic layer washed with 1N HCl (2×70 ml), water (3×70 ml), brine (2×50 ml), dried over Na2SO4, filtered, concentrated and dried to give 3-biphenyl-4-yl-acrylic acid (7.393 g, 32.966 mmol, 84%) as a white solid, dec. 223-226° C. 1H NMR (DMSO-d6) δ 6.58 (d, 1H), 7.37-7.53 (m, 3H), 7.62 (d, 1H), 7.70-7.84 (m, 6H), 12.40 (s, 1H); mass spectrum [ES(−)], m/z 223 (M−H)−.
後処理
- temperaturethe mixture refluxed
- temperatureheating
- concentrationThe reaction mixture was concentrated to about 50 ml
- additiondiluted with water (200 ml)
- additionEtOAc (1000 ml) was added
- temperaturethe whole mixture heated
- dissolutionto dissolve all solids
- temperatureAfter cooling
- customthe layers were separated
- washthe organic layer washed with 1N HCl (2×70 ml), water (3×70 ml), brine (2×50 ml)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customdried
出典と根拠
- ORDレコード
- ord-8a6ec0d1cadf4067844245e9ccae4d46
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07420083B2
関連ノート
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