Hydrochloric Acid → 2-Hydroxy-3-methyl-2-(trifluoromethyl)butan-1-aminium chloride

HRID 2202536

반응식

HRID 2202536 반응식
[F:1][C:2]([F:13])([F:12])[C:3]([CH2:8][N+:9]([O-])=O)([OH:7])[CH:4]([CH3:6])[CH3:5].[ClH:14]>CCO.CO.[Pd]>[Cl-:14].[OH:7][C:3]([C:2]([F:1])([F:12])[F:13])([CH:4]([CH3:6])[CH3:5])[CH2:8][NH3+:9]

참가 물질

6

실험 절차

To a solution of 1,1,1-trifluoro-3-methyl-2-(nitromethyl)butan-2-ol (753 mg, 3.74 mmol) in EtOH (10 ml) in a 25 ml medium pressure glass hydrogenation vessel under N2, 10% Pd on carbon (39.8 mg, 0.374 mmol) was added. The vessel was flushed with N2, followed by H2 (22.64 mg, 11.23 mmol) at 5 bar pressure and stirred at RT for 6 days. The mixture was filtered through Celite® and washed through with EtOH (30 ml), followed by DCM (10 ml). The filtrate was concentrated under vacuum to give a colourless oil. The crude product was taken up in methanol (20 ml) and treated with a 1.25M HCl in methanol solution. The resulting colourless solution was stirred at RT for 1 hour and concentrated under vacuum to afford the title compound;

후처리

  1. customThe vessel was flushed with N2
  2. filtrationThe mixture was filtered through Celite®
  3. washwashed through with EtOH (30 ml)
  4. concentrationThe filtrate was concentrated under vacuum
  5. customto give a colourless oil
  6. stirringThe resulting colourless solution was stirred at RT for 1 hour
  7. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-54464e2ed2eb4689bb92baca3a9f86e6
출처 데이터셋
uspto-grants-2016_06
특허 번호
US09365552B2

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