تفاعل #171307

ord-86209a96cdaa42ce870321d1ddeafa0e

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with EtOAc (200 mL)
  2. 2
    غسيلthe organic phase washed with saturated aqueous NaHCO3 (2×100 mL), brine (100 mL)
  3. 3
    تجفيفdried with Na2SO4
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe crude product was purified by flash chromatography (6% EtOAc in hexane, silica)

الإجراء التجريبي

A solution of N-trifluoroacetyl-8-chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (2.5 g, 8.5 mmol) in 1,2-dichloroethane (15 mL) was treated with Selectfluor (3.9 g, 11 mmol), trifluoromethanesulfonic acid (8 mL, 90 mmol) and stirred 60 hours at 75 C. The product mixture was poured into water (200 mL), extracted with EtOAc (200 mL), the organic phase washed with saturated aqueous NaHCO3 (2×100 mL), brine (100 mL), dried with Na2SO4 and concentrated. The crude product was purified by flash chromatography (6% EtOAc in hexane, silica) resulting in 1.6 g of a white solid. MS calculated for C13H12ClF4NO+H: 310, observed: 310.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08846906B2uspto-grants-2014_09