반응 #502080

ord-c2cff8fa61ed4eb5b88f54a2b7bc8ee4

반응 방정식

[Na+].[O-]Cl
sodium hypochlorite
ClCCl
Dichloromethane
CC(C)CCCC(C)OCCO
2-[(1,5-dimethylhexyl)oxy]ethanol
[Br-].[K+]
potassium bromide
CC(C)CCCC(C)OCC=O
oil
수율 78.1%
CC(C)CCCC(C)OCC=O
[(1,5-dimethylhexyl)oxy]acetaldehyde
수율 78.1%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타fitted with addition funnel, condenser
  2. 2
    추출The product was extracted with hexane (200 ml)
  3. 3
    세척washed with water (2×200 ml)
  4. 4
    건조The organic phase was dried over sodium sulphate
  5. 5
    여과filtered
  6. 6
    기타the solvent removed by evaporation

실험 절차

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%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08088725B2uspto-grants-2012_01