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Ammonium formate → Ethyl 2-(4-amino-3-hydroxyphenyl)acetate

HRID 49702
노트
인쇄 미리보기

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HRID 49702 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH:5]=[CH:6][C:7]=1[N+:8]([O-])=O.C([O-])=O.[NH4+]>C(O)C.[Pd]>[NH2:8][C:7]1[CH:6]=[CH:5][C:4]([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:3][C:2]=1[OH:1]
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참가 물질

5

반응물 2

HCID 2723923Ammonium formateHCID 23508320Ethyl 2-(3-hydroxy-4-nitrophenyl)acetate

생성물 1

HCID 23508323Ethyl 2-(4-amino-3-hydroxyphenyl)acetate수율 76.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

반응 조건

온도
50 °C

실험 절차

A solution of ethyl 3-hydroxy-4-nitrophenylacetate (5.0 g, Reference Example 4) was dissolved in ethanol (approximately 200 mL) was treated with ammonium formate (approximately 20 g). The mixture was warmed to 50° C. and then treated cautiously with palladium on charcoal (approximately 1 g, 5%)—effervescence was observed. After 30 minutes the mixture was filtered hot through a pad of celite and the filtrate was concentrated to give the title compound (3.3 g) as a black solid.

후처리

  1. filtrationAfter 30 minutes the mixture was filtered hot through a pad of celite
  2. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-2f21c1783ad945c5b97ae8938d3780b8
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706738B2

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