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
- customThe vessel was flushed with N2
- filtrationThe mixture was filtered through Celite®
- washwashed through with EtOH (30 ml)
- concentrationThe filtrate was concentrated under vacuum
- customto give a colourless oil
- stirringThe resulting colourless solution was stirred at RT for 1 hour
- concentrationconcentrated under vacuum
출처 및 근거
- ORD 기록
- ord-54464e2ed2eb4689bb92baca3a9f86e6
- 출처 데이터셋
- uspto-grants-2016_06
- 특허 번호
- US09365552B2
연결된 노트
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