反応式
[CH3:1][O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][C:7](Br)=[CH:6][C:5]=1[CH3:11].C(N(CC)CC)C.O.[C]=O.[C:23]([O:26]CC)(=[O:25])C>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C1(P(C(P(C2C=CC=CC=2)C2C=CC=CC=2)(C)C)C2C=CC=CC=2)C=CC=CC=1.C(#N)C>[CH3:1][O:2][C:3]([C:4]1[CH:9]=[CH:8][C:7]([C:23]([OH:26])=[O:25])=[CH:6][C:5]=1[CH3:11])=[O:12]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 3
反応条件
- 温度
- 83 °C
実験手順
A mixture of 4-bromo-2-methylbenzoic acid methyl ester (prepared by the literature method: Keuning, K. J.; Evenhuis, N. Recueil Trav. Chim. Pays-Bas 1935, 54, 73-75; 12.21 g, 53.3 mmol), triethylamine (16.00 g, 158.1 mmol), palladium(II) acetate (0.28 g, 1.25 mmol), bis(diphenylphosphino)propane (0.52 g, 1.26 mmol), water (16.00 g, 888.1 mmol) and acetonitrile (40 mL) was pressurized to 40 pounds per square inch with carbon monoxide and the pressure was released. After six such cycles, the bottle was pressurized again and the contents were stirred at 83° C. for 3 h. The reaction mixture was cooled to room temperature and depressurized. Ethyl acetate (100 mL) was added and the solution was filtered and then extracted with water (5×40 mL). The combined aqueous layers were acidified with 1N hydrochloric acid solution to pH 2 and the resulting mixture was extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with brine (200 mL), dried (MgSO4) and evaporated under reduced pressure to give 4-(methoxycarbonyl)-3-methylbenzoic acid as a colorless solid (4.83 g, 47% yield).
後処理
- customprepared by the literature method
- temperatureThe reaction mixture was cooled to room temperature
- filtrationthe solution was filtered
- extractionextracted with water (5×40 mL)
- extractionthe resulting mixture was extracted with ethyl acetate (2×100 mL)
- washThe combined organic layers were washed with brine (200 mL)
- dry with materialdried (MgSO4)
- customevaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-1b88ce79cbd944b2b96dd51dc7c43e6a
- 出典データセット
- uspto-grants-2003_02
- 特許番号
- US06515124B2
関連ノート
読み込み中…