2,2,5,5,-Tetramethylcyclopentanone → 2,2,5,5-Tetramethylcyclopentan-1-ol

HRID 2291397Notes

Reaction equation

HRID 2291397 reaction equation
[CH3:1][C:2]1([CH3:10])[CH2:6][CH2:5][C:4]([CH3:8])([CH3:7])[C:3]1=[O:9].[BH4-].[Na+]>CO.O>[CH3:1][C:2]1([CH3:10])[CH2:6][CH2:5][C:4]([CH3:8])([CH3:7])[CH:3]1[OH:9]

Participants

5

Conditions

Temperature
70 °C

Procedure

54.9 g of 2,2,5,5-tetramethylcyclopentanone was dissolved in a solvent mixture of 95 ml of methanol and 95 ml of water, and 24.0 g of sodium borohydride was added thereto. The mixture was stirred at 70° C. for 15 hours. The reaction solution was concentrated under reduced pressure, and 100 ml of water was added thereto. The mixture was twice extracted with 100 ml of chloroform, and the organic layers were combined and washed with 100 ml of an aqueous saturated sodium chloride solution. Then, the solution was concentrated under reduced pressure. The liquid residue was distilled under reduced pressure, whereby 43.25 g of 2,2,5,5-tetramethylcyclopentanol was obtained as a colorless oily substance (b.p. 40° C. / 3 mmHg).

Workup

  1. additionwas added
  2. concentrationThe reaction solution was concentrated under reduced pressure, and 100 ml of water
  3. additionwas added
  4. extractionThe mixture was twice extracted with 100 ml of chloroform
  5. washwashed with 100 ml of an aqueous saturated sodium chloride solution
  6. concentrationThen, the solution was concentrated under reduced pressure
  7. distillationThe liquid residue was distilled under reduced pressure

Sources & evidence

ORD record
ord-c989e2efe6654ad3a8fd5de8246b8e14
Source dataset
uspto-grants-1989_01
Patent number
US04795831

Reaction notes

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