反応式
OC1[CH:10]=[CH:9][CH:8]=[C:7]2C=1[CH2:4][CH2:5][C:6]2=[O:11].[H-].[Na+].[CH3:14]I.[CH2:16]1[CH2:20][O:19][CH2:18][CH2:17]1>>[CH3:14][C:5]1([CH3:4])[CH2:17][C:16]2[C:7](=[CH:8][CH:9]=[CH:10][C:20]=2[O:19][CH3:18])[C:6]1=[O:11]参加物
5
実験手順
4-Hydroxy-indanone (25 g) is added portionwise to a stirred suspension of sodium hydride (40.1 g, 60% in mineral oil) and methyl iodide (62.4 g) in anhydrous THF (990 ml) under nitrogen and the mixture is stirred at RT overnight. The reaction mixture is quenched with H2O, washed with diethyl ether and the etheral layer is washed with 10% aq. NaHSO3 and H2O, dried, filtered, and evaporated. The residue is chromatographed (silica gel; eluent=hexane/EtOAC) affording the desired product as a solid.
後処理
- customThe reaction mixture is quenched with H2O
- washwashed with diethyl ether
- washthe etheral layer is washed with 10% aq. NaHSO3 and H2O
- customdried
- filtrationfiltered
- customevaporated
- customThe residue is chromatographed (silica gel; eluent=hexane/EtOAC)
出典と根拠
- ORDレコード
- ord-bb2a6ed572d8406ab7a288aafce2c017
- 出典データセット
- uspto-grants-1987_10
- 特許番号
- US04699906
関連ノート
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