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3-(4-Methoxy-2-nitrophenyl)acrylic acid methyl ester → 7-Methoxy-3,4-dihydroquinolin-2(1H)-one

HRID 490694
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인쇄 미리보기

반응식

HRID 490694 반응식
C[O:2][C:3](=O)[CH:4]=[CH:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[CH:8][C:7]=1[N+:14]([O-])=O>CO.CCOC(C)=O.CCO.[Pd]>[CH3:13][O:12][C:9]1[CH:8]=[C:7]2[C:6]([CH2:5][CH2:4][C:3](=[O:2])[NH:14]2)=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 1

HCID 538271683-(4-Methoxy-2-nitrophenyl)acrylic acid methyl ester

생성물 1

HCID 128994187-Methoxy-3,4-dihydroquinolin-2(1H)-one수율 43.4%

시약·촉매·용매 4

HCID 23938Palladium촉매HCID 702Ethanol용매HCID 887Methanol용매HCID 8857Ethyl Acetate용매

실험 절차

A solution of 3-(4-methoxy-2-nitro-phenyl)-acrylic acid methyl ester (4.00 g, 16.9 mmol) in MeOH (100 mL) and EtOAc (20 mL) is added a slurry of Pd/C (200 mg) in EtOH (20 mL). The suspension is hydrogenated under a pressure of 60 psi for 12 hours. The mixture is then filter through a pad of celite and the filtrate is concentrated and purified on silica gel chromatography column with 30-40-50% EtOAc/Hexanes to obtain the title product (1.30 g, 43%) and an uncyclized by-product (0.60 g).

후처리

  1. filtrationThe mixture is then filter through a pad of celite
  2. concentrationthe filtrate is concentrated
  3. custompurified on silica gel chromatography column with 30-40-50% EtOAc/Hexanes

출처 및 근거

ORD 기록
ord-ba24b49f2b9643df8e7baaf775c09c06
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07528160B2

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