反応式
C([O:3][C:4]([C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[O:18][CH3:19])=[CH:8][CH:7]=1)=[O:5])C.[OH-].[Na+]>O1CCCC1>[CH3:19][O:18][C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=1[C:9]1[CH:10]=[CH:11][C:6]([C:4]([OH:5])=[O:3])=[CH:7][CH:8]=1参加物
4
実験手順
A mixture of 2′-methoxy-[1,1′-biphenyl]-4-carboxylic acid ethyl ester of Step A (3.7 g, 14.4 mmol) in tetrahydrofuran (40 mL) and 1 N sodium hydroxide (30 mL, 30 mmol) was heated at reflux overnight. After cooling, the reaction mixture was concentrated in vacuo, and the residue was acidified with 2N hydrochloric acid to give a white solid which was collected by filtration and dried under vacuum to provide the title compound (3.2 g, 97.4%) as a white solid, m.p. 250-253° C.
後処理
- temperaturewas heated
- temperatureat reflux overnight
- temperatureAfter cooling
- concentrationthe reaction mixture was concentrated in vacuo
- customto give a white solid which
- filtrationwas collected by filtration
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-f55b762bdda741a69d85a3996b200959
- 出典データセット
- uspto-grants-2005_06
- 特許番号
- US06903091B2
関連ノート
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