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

HRID 574811

反応式

HRID 574811 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-de4583a6a7d64e8da4f2080439da93cf
出典データセット
uspto-grants-2015_05
特許番号
US09034875B2

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