Rac-(1r,4r)-4-methoxycyclohexane-1-carboxylic acid → (4-Methoxycyclohexyl)methanol

HRID 1035915

反応式

HRID 1035915 の反応式
[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

  1. concentrationThe mixture was concentrated
  2. dissolutionthe residue was dissolved in methanol (100 mL)
  3. concentrationconcentrated
  4. dissolutionThe residue was dissolved in dichloromethane
  5. washwashed with water
  6. dry with materialThe organic layer was dried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-7e12cebf5b7c41e3bb4baf0e81312ea1
出典データセット
uspto-grants-2013_10
特許番号
US08546399B2

関連ノート

読み込み中…