Water → 2-(4-Bromophenyl)oxirane

HRID 1896178Notes

Reaction equation

HRID 1896178 reaction equation
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.[I-].[CH3:11][S+](C)C.O.[OH-].[K+]>C(#N)C>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]2[CH2:11][O:7]2)=[CH:4][CH:3]=1

Participants

6

Conditions

Temperature
55 °C

Procedure

A mixture of 4-bromobenzaldehyde (intermediate 29, 25.25 g, 136 mmol), trimethylsulfonium iodide (28.71 g, 141 mmol), water (6.5 ml, 361 mmol) and potassium hydroxide (15.56 g, 277 mmol) in acetonitrile (140 ml) was warmed to 55° C. for 2.5 hours. The resulting solution was partitioned between water and diethyl ether, and the organic layer was washed with water, diluted hydrochloric acid, and brine, and dried over sodium sulfate. Crude product of 2-(4-bromo-phenyl)-oxirane (intermediate 30) was obtained by removal of organic solvent under reduced pressure, which was used for next reaction without purification.

Workup

  1. customThe resulting solution was partitioned between water and diethyl ether
  2. washthe organic layer was washed with water, diluted hydrochloric acid, and brine
  3. dry with materialdried over sodium sulfate

Sources & evidence

ORD record
ord-d7cab41c7f8f456abd7dda259516473b
Source dataset
uspto-grants-2013_08
Patent number
US08518939B2

Reaction notes

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