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HCID 13265131, 화합물 → HCID 22105824, 화합물

HRID 1640004
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HRID 1640004 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH:10]([CH3:18])[C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])=[CH:6][CH:5]=1)([O-])=O>[Pd].C(O)C>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([CH:10]([CH3:18])[C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 13265131HCID 13265131, 화합물

생성물 1

HCID 22105824HCID 22105824, 화합물수율 99%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of tert-butyl 2-(4-nitrophenyl)propanoate (14.4 g, 57.3 mmol) and 10% palladium on carbon (1.44 g, 10% by weight) in ethanol (150 mL) was shaken under an atmosphere of hydrogen at 40 psi for 2 h. After this time, the reaction was filtered through diatomaceous earth, and concentrated under reduced pressure to afford tert-butyl 2-(4-aminophenyl)propanoate (12.5 g, 99%) as an orange oil: 1H NNR (300 MHz, CDCl3) δ 7.07 (d, J=9.1 Hz, 2H), 6.63 (d, J=9.1 Hz, 2H), 3.60 (s, 2H), 3.49 (q, J=7.1 Hz, 1H), 1.40 (d, 3H), 1.38 (s, 9H); ESI MS m/z 222 [M+H]+.

후처리

  1. filtrationAfter this time, the reaction was filtered through diatomaceous earth
  2. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-b45dc8b6cb6746eb9113f54c62be5560
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08110681B2

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