1-Phenyl-1-propanone → 1-Phenyl-1-propanol

HRID 1578038Notes

Reaction equation

HRID 1578038 reaction equation
Cl([O-])(=O)(=O)=O.[OH-].[K+].[C:8]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)(=[O:11])[CH2:9][CH3:10]>C(O)(C)C>[CH3:10][CH2:9][CH:8]([OH:11])[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1

Participants

5

Reactant 3

HCID 71481-Phenyl-1-propanoneHCID 14797Potassium HydroxideHCID 123351Perchlorate

Product 1

HCID 71471-Phenyl-1-propanol

Reagents, catalysts & solvents 1

HCID 3776IsopropanolSolvent2×

Procedure

6.1 mg (1×10-5 moles) of [Ir(PPEI)COD]+ClO4- (+) were suspended in 50 ml of isopropanol and oxidized with air for 4 hours. The yellow solution obtained was then degasified at reflux in a nitrogen stream for 20 minutes and then treated with 4.0 ml of an isopropanol solution of KOH (4 mg of KOH). The solution, after a preliminary reduction for 30 minutes at reflux in a nitrogen flow, was treated with 2.56 ml of deaerated propiophenone. After 180 minutes, a conversion to phenylpropanol (+) of 89.3% with an e.e. of 26.1% was obtained. Ratios:

Workup

  1. customThe yellow solution obtained
  2. temperatureat reflux in a nitrogen stream for 20 minutes
  3. temperatureThe solution, after a preliminary reduction for 30 minutes at reflux in a nitrogen flow
  4. waitAfter 180 minutes

Sources & evidence

ORD record
ord-3f4fa818b9204438a89165bb7a56f984
Source dataset
uspto-grants-1981_09
Patent number
US04290961

Reaction notes

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