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Ammonium formate → Ethyl 2-(propylamino)acetate

HRID 269468
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HRID 269468 반응식
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]
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참가 물질

5

반응물 2

HCID 2723923Ammonium formateHCID 69215857HCID 69215857, 화합물

생성물 1

HCID 13454968Ethyl 2-(propylamino)acetate

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 702Ethanol용매

반응 조건

온도
80 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-fa6f7639f6ec418a92090d02045e091c
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07446204B2

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