反応式
[OH-].[K+].[CH3:3][C:4]([C:7]1[CH:12]=[C:11]([SH:13])[CH:10]=[C:9]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:8]=1[OH:18])([CH3:6])[CH3:5].C([O:21][C:22](=[O:27])[CH2:23][CH2:24][CH2:25]Br)C.O>CC(C)=O>[CH3:6][C:4]([C:7]1[CH:12]=[C:11]([S:13][CH2:25][CH2:24][CH2:23][C:22]([OH:27])=[O:21])[CH:10]=[C:9]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:8]=1[OH:18])([CH3:3])[CH3:5]参加物
実験手順
Potassium hydroxide flakes (2.52 g, 0.045 mole) were added to a clear solution of 2,6-bis(1,1-dimethylethyl)-4-mercaptophenol (3.57 g, 0.0165 mole) and ethyl-4-bromo-butyrate (3.23 g, 0.0165 mole) in acetone (10 ml). Water (20 ml) was added and the solution stirred for 1.5 hours, the solvent removed on a rotary evaporator and water (50 ml) added, and the mixture was extracted with ethyl ether (3×75 ml). The aqueous layer was acidified with concentrated hydrochloric acid, extracted with ethyl ether (2×50 ml), the combined organic extracts were washed with water (50 ml), dried over sodium sulfate, filtered and the solvents removed, leaving an oil, which was purified by chromatography on silica, recrystallized from ethyl ether/Skellysolve B, filtered and the product dried in vacuo at room temperature for 12 hours, m.p. ca. 112°-113.5° C.
後処理
- customthe solvent removed on a rotary evaporator and water (50 ml)
- additionadded
- extractionthe mixture was extracted with ethyl ether (3×75 ml)
- extractionextracted with ethyl ether (2×50 ml)
- washthe combined organic extracts were washed with water (50 ml)
- dry with materialdried over sodium sulfate
- filtrationfiltered
- customthe solvents removed
- customleaving an oil, which
- customwas purified by chromatography on silica
- customrecrystallized from ethyl ether/Skellysolve B
- filtrationfiltered
- customthe product dried in vacuo at room temperature for 12 hours
出典と根拠
- ORDレコード
- ord-e382774d53ff40749e90ddad18853b83
- 出典データセット
- uspto-grants-1993_09
- 特許番号
- US05244899
関連ノート
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