Реакция #1269817

ord-908483dbc8ce4f128256e11f122f7aa9

Уравнение реакции

O=S(=O)(Cl)c1cc2ccccc2s1
benzo[b]thiophene-2-sulfonyl chloride
O=[N+]([O-])O
nitric acid
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
product
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
Mono nitro-benzo[b]thiophene-2-sulfonyl chloride

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe resulting mixture was refluxed overnight
  2. 2
    ДругоеThe organic layer was separated
  3. 3
    Экстракцияthe aqueous layer was extracted by 220 mL 2 dichloromethane
  4. 4
    Сушкаdried over MgSO4
  5. 5
    ДругоеSolvent was then removed by rotary evaporator
  6. 6
    ДругоеThe crude product was purified by flash column chromatography with an eluent of hexane

Методика

To a solution of benzo[b]thiophene-2-sulfonyl chloride (1.165 g, 5 mmol) in 25 mL of dichloromethane was added 3.6 mL of concentrated nitric acid (≧22.05 mol/L) dropwise, the resulting mixture was refluxed overnight and cooled to room temperature before it was poured into 20 gram of crushed ice. The organic layer was separated and the aqueous layer was extracted by 220 mL 2 dichloromethane. The organic layers were combined and dried over MgSO4. Solvent was then removed by rotary evaporator. The crude product was purified by flash column chromatography with an eluent of hexane, followed by a gradient eluent of hexane/ethyl acetate (6/1-3/1) to afford 0.58 g of product (mixture of 65% of 4-nitro-benzo[b]thiophene-2-sulfonyl chloride and 35% of 7-nitro-benzo[b]thiophene-2-sulfonyl chloride).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08663901B2uspto-grants-2014_03