Methanol → 2-(Isopropylthio)aniline

HRID 363245노트

반응식

HRID 363245 반응식
Cl[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([N+:8]([O-])=O)[C:3]=1[S:11][CH:12]([CH3:14])[CH3:13].CO.[H][H]>[Ni].O>[CH:12]([S:11][C:3]1[CH:2]=[CH:7][CH:6]=[CH:5][C:4]=1[NH2:8])([CH3:14])[CH3:13]

참가 물질

6

반응 조건

온도
60 °C

실험 절차

34.7 g of 2-chloro-6-nitrophenyl-isopropylsulfane, 140.0 g of methanol and 1 g of Raney nickel 55, as the catalyst (water-moist), were initially introduced into a 0.3 l steel autoclave. After the air had been displaced with nitrogen and hydrogen, hydrogen was forced in at room temperature up to a pressure of 80 bar, while stirring the mixture, a slight increase in temperature already being observed. The mixture was heated to 60° C., while continuing to stir and keep the hydrogen pressure constant. After about 2 hours, the uptake of hydrogen had ended. The mixture was then cooled to room temperature, the hydrogen was let down, the catalyst was filtered off with suction and washed with methanol and the combined filtrates were concentrated. Crude yield: 29.6 g of 2-amino-6-chlorophenyl-isopropylsulfane with a purity of 99.5% (GC), corresponding to 97.5% of theory. The content of 2-isopropylmercaptoaniline formed by hydrogenating dehalogenation was only 0.1%. Furthermore, only 0.1% of impurities due to 3-chloroaniline, formed by hydrogenating desulfurization, were found.

후처리

  1. customwas forced in at room temperature up to a pressure of 80 bar
  2. temperaturea slight increase in temperature
  3. stirringto stir
  4. temperatureThe mixture was then cooled to room temperature
  5. filtrationthe catalyst was filtered off with suction
  6. washwashed with methanol
  7. concentrationthe combined filtrates were concentrated

출처 및 근거

ORD 기록
ord-86f207fb450945e1811661924f4c3cf9
출처 데이터셋
uspto-grants-1999_02
특허 번호
US05872300

반응 노트

불러오는 중…