Реакция #3846

ord-032d77276ec347c0b8611cfd56e26b51

Уравнение реакции

C=CCBr
Allyl bromide
O=S(=O)(Nc1ccccc1C(F)(F)F)c1cccc[n+]1[O-]
N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide
[H-].[Na+]
NaH
C=CCN(c1ccccc1C(F)(F)F)S(=O)(=O)c1cccc[n+]1[O-]
title compound
C=CCN(c1ccccc1C(F)(F)F)S(=O)(=O)c1cccc[n+]1[O-]
N-allyl-N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGthe mixture is stirred at RT for 48 hours
  2. 2
    Другоеpurified

Методика

To N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide (compound 129, Table A) (1.0 g, 3.0 mmol) in 10 ml of DMF is added NaH (0.30 g, 6.2 mmol) under N2, and the mixture is stirred at RT for 30 minutes. Allyl bromide (0.82 g, 0.59 ml, 6.8 mmol) is added dropwise, and the mixture is stirred at RT for 48 hours. It is then worked up and purified to give the title compound (compound 37, Table A). (DMF is dimethylformamide; RT is room temperature.)

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04722749uspto-grants-1988_02