反応 #2186211

ord-0e28e73e13c248f985c6c582f3f7c17e

反応方程式

Cl
hydrochloric acid
[Mg]
magnesium
Clc1ccccc1
chlorobenzene
C[Si](C)(C)Cl
trimethylsilyl chloride
O=S(c1ccccc1)c1ccccc1
Diphenyl sulfoxide
[Cl-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
triphenylsulfonium chloride

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONwas added dropwise at a temperature below 20° C
  2. 2
    workup.WAITto mature for one hour
  3. 3
    その他to quench
  4. 4
    その他the reaction
  5. 5
    その他The water layer was separated
  6. 6
    洗浄washed with 100 g of diethyl ether

実験手順

Diphenyl sulfoxide, 40 g (0.2 mole), was dissolved in 400 g of dichloromethane, which was stirred under ice cooling. At a temperature below 20° C., 65 g (0.6 mole) of trimethylsilyl chloride was added dropwise to the solution, which was allowed to mature for 30 minutes at the temperature. Then, a Grignard reagent which had been prepared from 14.6 g (0.6 mole) of metallic magnesium, 67.5 g (0.6 mole) of chlorobenzene and 168 g of tetrahydrofuran (THF) was added dropwise at a temperature below 20° C. The reaction solution was allowed to mature for one hour, after which 50 g of water at a temperature below 20° C. was added to quench the reaction. To this solution, 150 g of water, 10 g of 12N hydrochloric acid, and 200 g of diethyl ether were further added. The water layer was separated and washed with 100 g of diethyl ether, yielding an aqueous solution of triphenylsulfonium chloride. The compound in aqueous solution form was used in the subsequent reaction without further isolation.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07569326B2uspto-grants-2009_08