反応式
[CH3:1][O:2][CH:3]1[CH2:8][CH2:7][CH:6]([C:9](O)=[O:10])[CH2:5][CH2:4]1>O1CCCC1>[CH3:1][O:2][CH:3]1[CH2:8][CH2:7][CH:6]([CH2:9][OH:10])[CH2:5][CH2:4]1参加物
3
実験手順
4-Methoxycyclohexanecarboxylic acid (7 g) in tetrahydrofuran (20 mL) was treated with 1 M (in tetrahydrofuran) borane-tetrahydrofuran complex (100 mL) overnight. The mixture was concentrated and the residue was dissolved in methanol (100 mL) and concentrated HCl (10 mL). The resulting mixture was stirred for 1 hour and concentrated. The residue was dissolved in dichloromethane and washed with water. The organic layer was dried over Na2SO4, filtered, and concentrated to give the title compound.
後処理
- concentrationThe mixture was concentrated
- dissolutionthe residue was dissolved in methanol (100 mL)
- concentrationconcentrated
- dissolutionThe residue was dissolved in dichloromethane
- washwashed with water
- dry with materialThe organic layer was dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-de4583a6a7d64e8da4f2080439da93cf
- 出典データセット
- uspto-grants-2015_05
- 特許番号
- US09034875B2
関連ノート
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