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Ammonium formate → Ethyl 2-(propylamino)acetate

HRID 269468
ノート
印刷プレビュー

反応式

HRID 269468 の反応式
C([O-])=O.[NH4+].C([CH2:12][CH2:13][CH2:14][NH:15][CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])C1C=CC=CC=1>C(O)C.C(O)(=O)C>[CH2:14]([NH:15][CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH2:13][CH3:12]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 2723923Ammonium formateHCID 69215857HCID 69215857、化合物

生成物 1

HCID 13454968Ethyl 2-(propylamino)acetate

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 702Ethanol溶媒

反応条件

温度
80 °C

実験手順

Ammonium formate (2 g, 31 mmol) was added to a solution of ethyl 2-[benzylpropylamino]acetate (1.05 g, 4.47 mmol) in ethanol (15 mL) and acetic acid (1 mL). The reaction vessel was then carefully flushed with nitrogen gas. Palladium on carbon (10%, 300 mg) was added in one portion, and the resulting mixture was heated at 80° C., under nitrogen for 3 h. The reaction mixture was allowed to cool to room temperature, and filtered through celite filteraid. The filtrate was concentrated in vacuo, (azeotroping with toluene (20 mL) to remove the acetic acid), to give ethyl 2-(propylamino)acetate as a yellow oil (quantitative crude yield). 1H NMR (CDCl3) δ 4.14 (q, J=7.1 Hz, 2H), 3.30 (s, 2H), 2.60 (dd, J=7.4 Hz, 2H), 1.50 (m, 2H), 1.26 (t, J=7.2 Hz, 3H), 0.89 (t, J=7.4 Hz, 3H).

後処理

  1. customThe reaction vessel was then carefully flushed with nitrogen gas
  2. additionPalladium on carbon (10%, 300 mg) was added in one portion
  3. temperatureto cool to room temperature
  4. filtrationfiltered through celite filteraid
  5. concentrationThe filtrate was concentrated in vacuo
  6. custom(azeotroping with toluene (20 mL)
  7. customto remove the acetic acid),
  8. customto give

出典と根拠

ORDレコード
ord-fa6f7639f6ec418a92090d02045e091c
出典データセット
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07446204B2

反応ノート

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