Реакция #84802

ord-3f11c66f286c44a897ef57d806c4b40a

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe exothermic reaction
  2. 2
    Температураwas cooled briefly over a cold H2O bath
  3. 3
    Экстракцияextracted with EtOAc
  4. 4
    ПромывкаThe combined organics were washed with 1 M HCl, H2O and brine
  5. 5
    Сушкаthen dried over Na2SO4
  6. 6
    Концентрированиеconcentrated in vacuo

Методика

To a solution of methyl 2-(4-aminophenyl)-2-methoxyacetate (0.6 g, 3.07 mmol) in anhydrous pyridine (6 mL) under argon was added 3-chloropropane-1-sulfonyl chloride (0.5 mL, 4.11 mmol) dropwise. The exothermic reaction was cooled briefly over a cold H2O bath. After stirring for 1 hr, the reaction was diluted with H2O, 1 M HCl and brine and extracted with EtOAc. The combined organics were washed with 1 M HCl, H2O and brine then dried over Na2SO4 and concentrated in vacuo to give methyl 2-(4-(3-chloropropylsulfonamido)phenyl)-2-methoxyacetate as an orange oil (1.03 g, quant. yield). The product was used without further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09434707B2uspto-grants-2016_09