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HCID 21639277、化合物 → 3-Pyrrolidinepropanol

HRID 2095393
ノート
印刷プレビュー

反応式

HRID 2095393 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 21639277HCID 21639277、化合物

生成物 1

HCID 183371843-Pyrrolidinepropanol収率 85%

試薬・触媒・溶媒 2

HCID 345198Adams' catalyst触媒HCID 176Acetic Acid溶媒

実験手順

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+).

後処理

  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

出典と根拠

ORDレコード
ord-5ede1e9b3d7443a8aef4c84955cbae28
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08445684B2

反応ノート

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