反応式
[H-].[Na+].[C:3]([C:8]1[CH:13]=[C:12]([C:14]([CH2:17][CH3:18])([CH3:16])[CH3:15])[CH:11]=[CH:10][C:9]=1[OH:19])([CH2:6][CH3:7])([CH3:5])[CH3:4].Br[C:21]1[CH:30]=[CH:29][C:28](OC)=[CH:27][C:22]=1[C:23]([O:25][CH3:26])=[O:24].CCCCCCC.[CH2:40]([O:42][CH2:43]C)C>N1C=CC=CC=1.[Cu]Cl.C(OCC)(=O)C>[C:3]([C:8]1[CH:13]=[C:12]([C:14]([CH2:17][CH3:18])([CH3:16])[CH3:15])[CH:11]=[CH:10][C:9]=1[O:19][C:21]1[CH:30]=[CH:29][C:28]([CH2:40][O:42][CH3:43])=[CH:27][C:22]=1[C:23]([O:25][CH3:26])=[O:24])([CH2:6][CH3:7])([CH3:5])[CH3:4]参加物
実験手順
To a solution of sodium hydride (1.2 g, 0.05 mol) in pyridine (60 mL), was added a solution of 2,4-di-tert-pentylphenol (12.9 g, 0.055 mol) in pyridine (20 mL) with stirring. Gas evolution ceased in approximately 1.5 hr at which time methyl 2-bromo-5-methoxylbenzoate was added. Copper (I) chloride (1.24 g, 0.0126 mol) was added and the mixture heated to reflux for 8 hours. The reaction mixture was diluted with diethyl ether (100 mL) and washed with 3N HCl (3×50 mL) and then washed with saturated sodium bicarbonate (1×50 mL). The organic extracts were dried over sodium sulfate, filtered and concentrated to give a dark oil. Chromatography on silica gel with 1:1 heptane:ethyl acetate yielded the pure product as a viscous oil in 90% yield. NMR and mass spectral analysis were consistent with proposed structure.
後処理
- additionwas added
- temperaturethe mixture heated
- temperatureto reflux for 8 hours
- washwashed with 3N HCl (3×50 mL)
- washwashed with saturated sodium bicarbonate (1×50 mL)
- dry with materialThe organic extracts were dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto give a dark oil
出典と根拠
- ORDレコード
- ord-26886d3d31674d648fabaee48036271f
- 出典データセット
- uspto-grants-1993_11
- 特許番号
- US05258407
関連ノート
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