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Methanol → (-)-cis-N-[2-(3,4-Dimethoxyphenyl)cyclohexyl]-4-propionylbenzamide

HRID 1016280
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HRID 1016280 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C@@H:9]2[CH2:14][CH2:13][CH2:12][CH2:11][C@@H:10]2[N+:15]([O-])=O)=[CH:5][C:4]=1[O:18][CH3:19].[OH2:20].NN.[CH3:23][OH:24]>[Ni]>[CH3:19][O:18][C:4]1[CH:5]=[C:6]([C@H:9]2[CH2:14][CH2:13][CH2:12][CH2:11][C@H:10]2[NH:15][C:23](=[O:24])[C:3]2[CH:8]=[CH:7][C:6]([C:9](=[O:20])[CH2:10][CH3:11])=[CH:5][CH:4]=2)[CH:7]=[CH:8][C:3]=1[O:2][CH3:1]
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참가 물질

5

반응물 3

HCID 887MethanolHCID 24654Hydrazine hydrate (1:1)HCID 15389590(+/-)-cis1,2-Dimethoxy-4-(2-nitrocyclohexyl)benzene

생성물 1

HCID 53868529(-)-cis-N-[2-(3,4-Dimethoxyphenyl)cyclohexyl]-4-propionylbenzamide

시약·촉매·용매 1

HCID 935Nickel촉매

실험 절차

8.5 g of (+/−)-cis-1,2-dimethoxy-4-(2-nitrocyclohexyl)benzene are dissolved in 400 ml of methanol and treated at RT with 7 ml of hydrazine hydrate and 2.5 g of Raney nickel in portions in the course of 8 h. After stirring overnight at RT, the reaction mixture is filtered, the filtrate is concentrated and the residue is chromatographed on silica gel using a mixture of toluene/ethyl acetate/triethylamine=4/2/0.5. The title compound is obtained as an oil.

후처리

  1. filtrationthe reaction mixture is filtered
  2. concentrationthe filtrate is concentrated
  3. customthe residue is chromatographed on silica gel using
  4. additiona mixture of toluene/ethyl acetate/triethylamine=4/2/0.5

출처 및 근거

ORD 기록
ord-df0caf3b1288468981385b5f6c071991
출처 데이터셋
uspto-grants-2002_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06476025B1

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