Реакция #1605856

ord-d25c01dbd6d74b7f9680399f17365de5

Уравнение реакции

O
water
COc1ccc(CCl)cc1
p-methoxybenzyl chloride
CS(N)(=O)=O
methanesulfonamide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
COc1ccc(CN(Cc2ccc(OC)cc2)S(C)(=O)=O)cc1
title compound
Выход 97.0%
COc1ccc(CN(Cc2ccc(OC)cc2)S(C)(=O)=O)cc1
N,N-bis(4-methoxybenzyl)methanesulfonamide
Выход 97.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe resultant reaction mixture
  2. 2
    Другоеthe resultant reaction mixture
  3. 3
    workup.STIRRINGwas stirred at room temperature for 19 hours
  4. 4
    Экстракцияthe mixture was extracted with ethyl acetate
  5. 5
    СушкаThe obtained organic phase was dried over anhydrous sodium sulfate
  6. 6
    workup.DISTILLATIONFrom the organic phase, the solvent was distilled off under reduced pressure

Методика

To a solution of methanesulfonamide (5 g) in N,N-dimethylformamide (75 mL), potassium carbonate (29.1 g) was added and the resultant reaction mixture was stirred at room temperature for 5 hours. To the solution, p-methoxybenzyl chloride (18.1 g) was added and the resultant reaction mixture was stirred at room temperature for 19 hours. To the reaction solution, water was added and the mixture was extracted with ethyl acetate. The obtained organic phase was dried over anhydrous sodium sulfate. From the organic phase, the solvent was distilled off under reduced pressure to give the title compound (17.1 g) as a white solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09072758B2uspto-grants-2015_07