반응 #84341

ord-40d85bc262e84de38ac530141e6dc2dd

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타After completion of the reaction
  2. 2
    기타the solvent was evaporated under reduced pressure
  3. 3
    기타the resulting residue was purified by silica gel column chromatography

실험 절차

To 1.3 g of 2-bromo-1-[3-chloro-5-(2,2,2-trifluoroethoxy)pyridin-2-yl]ethanone in 10 ml of ethanol, 362 mg of methoxyamine hydrochloride was added, and the mixture was stirred at room temperature for 13 hours. After completion of the reaction, the solvent was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography using ethyl acetate-hexane (with a gradient of from 0:100 to 5:95) to obtain 1.2 g of the desired product as a colorless oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09434684B2uspto-grants-2016_09