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HCID 21639277, 화합물 → 3-Pyrrolidinepropanol

HRID 2095393
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HRID 2095393 반응식
[NH:1]1[CH:5]=[CH:4][C:3]([CH2:6][CH2:7][CH2:8][OH:9])=[CH:2]1>[Pt](=O)=O.C(O)(=O)C>[NH:1]1[CH2:5][CH2:4][CH:3]([CH2:6][CH2:7][CH2:8][OH:9])[CH2:2]1
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참가 물질

4

반응물 1

HCID 21639277HCID 21639277, 화합물

생성물 1

HCID 183371843-Pyrrolidinepropanol수율 85%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 176Acetic Acid용매

실험 절차

A solution of 3-(1H-pyrrol-3-yl)-1-propanol (400 mg, 3.20 mmol) in 5 mL of freshly distilled glacial acetic acid containing 40 mg of platinum(IV) oxide was hydrogenated with a H2 balloon for 2 h at 35° C. The catalyst was removed by filtration, and the solvent was evaporated. The residue was heated under reflux for 0.5 h with 4 mL of 30% aqueous NaOH solution to saponify any acetate ester that may have formed. The mixture was extracted with CH2Cl2, and the organic phase was concentrated to obtain the crude pyrrolidine (0.35 g, 85%) as a light-yellow oil, which could be used without purification in the following step. 1H NMR (CDCl3, 300 MHz) δ 3.66 (t, 2H, J=6.3 Hz), 2.62 (dd, 1H, J=7.2, 10.5 Hz), 2.91-2.99 (m, 2H), 2.51 (dd, 1H, J=7.2, 10.8 Hz), 1.93-2.15 (m, 2H), 1.56-1.65 (m, 2H), 1.46 (t, 2H, J=7.2 Hz), 1.37-1.41 (m, 2H). LC-MS (ESI) m/z 130 (M+H+).

후처리

  1. customThe catalyst was removed by filtration
  2. customthe solvent was evaporated
  3. temperatureThe residue was heated
  4. temperatureunder reflux for 0.5 h with 4 mL of 30% aqueous NaOH solution
  5. custommay have formed
  6. extractionThe mixture was extracted with CH2Cl2
  7. concentrationthe organic phase was concentrated

출처 및 근거

ORD 기록
ord-5ede1e9b3d7443a8aef4c84955cbae28
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08445684B2

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