Water → 2-(4-Bromophenyl)oxirane

HRID 218330Notes

Reaction equation

HRID 218330 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-7a80e117d0854487bca9ef48047048b7
Source dataset
uspto-grants-2012_06
Patent number
US08198437B2

Reaction notes

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