Potassium Bromide → 3-Methyl-5-cyclohexylpentanal

HRID 565191Notes

Reaction equation

HRID 565191 reaction equation
[CH3:1][CH:2]([CH2:6][CH2:7][CH:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1)[CH2:3][CH2:4][OH:5].[Br-].[K+].Cl[O-].[Na+].C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1.CC1(C)N([O])C(C)(C)CCC1.O>[CH3:1][CH:2]([CH2:6][CH2:7][CH:8]1[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]1)[CH2:3][CH:4]=[O:5]

Participants

8

Procedure

To a cooled (0° C.) mixture of 3-methyl-5-cyclohexylpentanol (50 g, 0.27 mol), water (50 ml), potassium bromide (3.2 g), and 1 mol % TEMPO (0.4 g) in 150 ml of toluene was added aqueous sodium hypochlorite (12% available chlorine, 167 g), buffered to pH=9.6 with 2.4 g of sodium bicarbonate over a period of 30 minutes. The reaction mixture was warmed to room temperature and stirred for 15 minutes. The organic layer was separated and washed sequentially with 250 ml KI solution (4.4 g of KI, 18 ml of 36% HCl, diluted to 250 ml), 50 ml of 5% sodium thiosulfate, and 50 ml of saturated aqueous sodium chloride. The organic phase was dried with magnesium sulfate and roto-evaporated to remove the toluene. The residue was distilled at 80° C. and 0.5 mmHg to yield the product (40 g, 80% yield) as a clear liquid. MS (EI) m/z (relative intensity) 182 (M+).

Workup

  1. temperatureTo a cooled
  2. customThe organic layer was separated
  3. washwashed sequentially with 250 ml KI solution (4.4 g of KI, 18 ml of 36% HCl, diluted to 250 ml), 50 ml of 5% sodium thiosulfate, and 50 ml of saturated aqueous sodium chloride
  4. dry with materialThe organic phase was dried with magnesium sulfate
  5. customroto-evaporated
  6. customto remove the toluene
  7. distillationThe residue was distilled at 80° C.

Sources & evidence

ORD record
ord-92c62420ee6049c4861278a94eb338d0
Source dataset
uspto-grants-2001_01
Patent number
US06172016B2

Reaction notes

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