Dimethyl Sulfoxide → 2,2-Difluoro-5-methoxy-1-pentanal hydrate

HRID 568980

반응식

HRID 568980 반응식
CS(C)=[O:3].C(Cl)(=O)C(Cl)=O.[F:11][C:12]([F:20])([CH2:15][CH2:16][CH2:17][O:18][CH3:19])[CH2:13][OH:14].C(N(CC)CC)C>ClCCl>[OH2:3].[F:11][C:12]([F:20])([CH2:15][CH2:16][CH2:17][O:18][CH3:19])[CH:13]=[O:14]

참가 물질

6

반응 조건

온도
-60 °C

실험 절차

A solution of dry dimethylsulfoxide (3 g, 38 mmoles) in dry dichloromethane (15 ml) is slowly added to a solution of oxalyl chloride (2.4 g, 19 mmoles) in dichloromethane (15 ml), kept under nitrogen and cooled to -60° C. Stirring is continued for 15 min. at -60° C. and followed by addition of 2,2-difluoro-1-hydroxy-5-methoxypentane (2.7 g, 17.5 mmoles) in dichloromethane (15 ml). The reaction mixture is stirred for 11/2 hours at -60° C., triethylamine (8.4 ml, 114 mmoles) in dichloromethane (15 ml) is slowly added, and the cooling bath is removed. The reaction mixture is hydrolyzed with brine and diluted with dichloromethane. The organic phase is then washed successively with 2N HCl containing some sodium chloride, and brine. Usual work-up affords the title compound (1.59 g, 53%) which is used for the next step without further purification.

후처리

  1. stirringThe reaction mixture is stirred for 11/2 hours at -60° C.
  2. customthe cooling bath is removed
  3. additiondiluted with dichloromethane
  4. washThe organic phase is then washed successively with 2N HCl containing some sodium chloride, and brine

출처 및 근거

ORD 기록
ord-7857d77b235a47458505ec6d65fe4927
출처 데이터셋
uspto-grants-1988_03
특허 번호
US04730006

연결된 노트

불러오는 중…