Acetic Acid → 3-Piperidin-3-ylpropan-1-ol
반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][CH2:8][CH2:9][OH:10])[CH:2]=1.CC(O)=O.Cl.CCO>O.[Pt](=O)=O.O>[NH:1]1[CH2:6][CH2:5][CH2:4][CH:3]([CH2:7][CH2:8][CH2:9][OH:10])[CH2:2]1참가 물질
실험 절차
A 500 mL Parr hydrogenation bottle was charged with 3-Pyridinepropanol (10.0 g, 72.9 mmol), platinum(IV)oxide hydrate (Adam's Catalyst) (500 mg), AcOH (30 mL), and HCl, 37% (1 mL). Contents of the bottle were hydrogenated at 47 psi for three days. EtOH and water were added, and the reaction mixture was filtered through CELITE. NaOH (10 N) was added and the mixture was extracted with methylene chloride, dried with anhydrous MgSO4, filtered and concentrated. The product was concentrated from PhMe and used without further purification. 1H NMR (CD3OD): δ 3.55 (t, J=5 Hz, 2H), 3.0{tilde over (5)} 2.95 (m, 2H), 2.5{tilde over (5)} 2.45 (m, 1H), 2.23 (t, J=10 Hz, 1H), 1.8 9 1.86 (m, 1H), 1.7{tilde over (0)} 1.66 (m, 1H), 1.6 0 1.44 (m, 4H), 1.2{tilde over (8)} 1.22 (m, 2H), 1.0 6 1.00 (m, 1H) ppm.
후처리
- filtrationthe reaction mixture was filtered through CELITE
- additionNaOH (10 N) was added
- extractionthe mixture was extracted with methylene chloride
- dry with materialdried with anhydrous MgSO4
- filtrationfiltered
- concentrationconcentrated
- concentrationThe product was concentrated from PhMe
- customused without further purification
출처 및 근거
- ORD 기록
- ord-e4a8139c66f045edb010d4c57cc3fb25
- 출처 데이터셋
- uspto-grants-2013_11
- 특허 번호
- US08591878B2
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