2-Octanol → 2-Octanone

HRID 1272590Notes

Reaction equation

HRID 1272590 reaction equation
[CH3:1][CH:2]([OH:9])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].C(=O)([O-])O.[Na+].C1C(=O)N(Br)C(=O)C1>CC1(C)N([O])C(C)(C)CCC1.ClCCCl>[CH3:1][C:2](=[O:9])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]

Participants

6

Reactant 3

HCID 200832-OctanolHCID 67184N-bromobutanimideHCID 516892Sodium Bicarbonate

Product 1

HCID 80932-OctanoneYield 95.2%

Reagents, catalysts & solvents 2

HCID 2724126TempoCatalystHCID 111,2-DichloroethaneSolvent

Procedure

2-Octanol (2.0 g, 15.4 mmol), sodium hydrogencarbonate (1.6 g, 18.5 mmol), TEMPO (24 mg, 0.15 mmol) and 1,2-dichloroethane (15 ml) were put in a 50-ml egg plant type flask. The suspension was cooled to less than 10° C. in an ice water bath, and thereto was added NBS (3.0 g, 16.9 mmol) divided in two portions. The insoluble materials were filtered off and the filtrate was washed with 5% aqueous sodium bicarbonate solution. The crude product was purified by distillation to give 2-octanone (1.88 g, yield 95%).

Workup

  1. temperatureThe suspension was cooled to less than 10° C. in an ice water bath
  2. filtrationThe insoluble materials were filtered off
  3. washthe filtrate was washed with 5% aqueous sodium bicarbonate solution
  4. distillationThe crude product was purified by distillation

Sources & evidence

ORD record
ord-20459be9627c474db74dc07a1e1b1e29
Source dataset
uspto-grants-2007_04
Patent number
US07208634B2

Reaction notes

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