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4-Hydroxy-3-nitro-5-[(1E)-prop-1-en-1-yl]benzonitrile → 3-Amino-4-hydroxy-5-propylbenzonitrile

HRID 2093628
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HRID 2093628 반응식
[OH:1][C:2]1[C:9](/[CH:10]=[CH:11]/[CH3:12])=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[N+:13]([O-])=O>C(OCC)(=O)C.[Pd]>[NH2:13][C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([CH2:10][CH2:11][CH3:12])[C:2]=1[OH:1])[C:6]#[N:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 687853344-Hydroxy-3-nitro-5-[(1E)-prop-1-en-1-yl]benzonitrile

생성물 1

HCID 687414503-Amino-4-hydroxy-5-propylbenzonitrile수율 26%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 1.78 g of 4-hydroxy-3-nitro-5-[(1E)-prop-1-en-1-yl]benzonitrile in ethyl acetate (10 ml) was added palladium on carbon (100 mg). This mixture was evacuated and flushed with hydrogen (via balloon) 10 times. The reaction was stirred at room temperature for 14 h under hydrogen. The mixture was then filtered through a plug of Celite, eluting with methanol. After concentration of the eluent in vacuo, the residue was further purified by column chromatography on a Biotage Horizon, eluting with 1 column volume of 100% hexanes followed by a gradient of 0-20% ethyl acetate in hexanes over 10 column volumes to provide the title compound (400 mg, 26%). Mass spectrum (ESI) 177.2 (M+1).

후처리

  1. customThis mixture was evacuated
  2. customflushed with hydrogen (via balloon) 10 times
  3. filtrationThe mixture was then filtered through a plug of Celite
  4. washeluting with methanol
  5. customAfter concentration of the eluent in vacuo, the residue was further purified by column chromatography on a Biotage Horizon
  6. washeluting with 1 column volume of 100% hexanes

출처 및 근거

ORD 기록
ord-71ac7e3b36c5490995e3a321899867ed
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08445480B2

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