Dichloromethane → HCID 86642025, compound

HRID 414898Notes

Reaction equation

HRID 414898 reaction equation
ClCCl.[CH3:4][CH:5]([O:12][CH2:13][CH2:14][OH:15])[CH2:6][CH2:7][CH2:8][CH:9]([CH3:11])[CH3:10].[Br-].[K+].Cl[O-].[Na+]>O>[CH3:4][CH:5]([O:12][CH2:13][CH:14]=[O:15])[CH2:6][CH2:7][CH2:8][CH:9]([CH3:10])[CH3:11]

Participants

6

Procedure

Dichloromethane (25 mL), 2-[(1,5-dimethylhexyl)oxy]ethanol (5 g, 29 mmol), a solution of potassium bromide (0.34 g, 2.9 mmol) in water (4.72 g) and 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO, 0.053 g, 0.34 mmol) was charged to 100 mL flask fitted with addition funnel, condenser, nitrogen, thermocouple and mechanical stirrer. A 2.8 wt % aqueous solution of sodium hypochlorite (173.5 g, 65 mmol) was added and the reaction stirred for a total of 15 hrs. The product was extracted with hexane (200 ml) and washed with water (2×200 ml). The organic phase was dried over sodium sulphate, filtered and the solvent removed by evaporation to yield a colourless oil (3.9 g). This oil (2 g) was chromatographed over silica gel (methyltert-butyl ether/hexane) to yield the product as a colourless oil (1.18 g, equating to a total chemical yield of 25%).

Workup

  1. customfitted with addition funnel, condenser
  2. extractionThe product was extracted with hexane (200 ml)
  3. washwashed with water (2×200 ml)
  4. dry with materialThe organic phase was dried over sodium sulphate
  5. filtrationfiltered
  6. customthe solvent removed by evaporation

Sources & evidence

ORD record
ord-c2cff8fa61ed4eb5b88f54a2b7bc8ee4
Source dataset
uspto-grants-2012_01
Patent number
US08088725B2

Reaction notes

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