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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2,4-Dichloro-1-(1-methoxy-2-nitro-propyl)-benzene → 1-(2,4-Dichlorophenyl)-1-methoxypropan-2-amine

HRID 1873863
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HRID 1873863 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH:9]([O:15][CH3:16])[CH:10]([N+:12]([O-])=O)[CH3:11]>C1COCC1.[Ni].CCO>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH:9]([O:15][CH3:16])[CH:10]([NH2:12])[CH3:11]
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참가 물질

4

반응물 1

HCID 584436852,4-Dichloro-1-(1-methoxy-2-nitro-propyl)-benzene

생성물 1

HCID 594032951-(2,4-Dichlorophenyl)-1-methoxypropan-2-amine수율 100%

시약·촉매·용매 2

HCID 86745698ethanol Raney-nickel촉매HCID 8028Tetrahydrofuran용매

실험 절차

2,4-dichloro-1-(1-methoxy-2-nitro-propyl)-benzene (132.2 g, 0.500 mol), was dissolved in THF (3.6 l). The solution was deaerated, RaNi-EtOH (133 g) catalyst was added, and the mixture was hydrogenated at 50 bar at ambient temperature for 23 hours. The catalyst was removed by filtration and the solvent was removed under reduced pressure. 117.1 g (100% of theory) of 2-(2,4-dichlorophenyl)-2-methoxy-1-methyl-ethylamine (compound Z1.14) was obtained in the form of a colourless oil as a mixture of diastereomeres.

후처리

  1. customThe catalyst was removed by filtration
  2. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-b17ba39f1a224e61907c0bb15c8992e0
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08304444B2

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