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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-(4-Nitrophenylmethyl)-thiomorpholine-1-oxide → 4-(4-Aminophenylmethyl)-thiomorpholine-1-oxide

HRID 24918
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인쇄 미리보기

반응식

HRID 24918 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][N:11]2[CH2:16][CH2:15][S:14](=[O:17])[CH2:13][CH2:12]2)=[CH:6][CH:5]=1)([O-])=O>[Ni].ClCCl.CO>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][N:11]2[CH2:16][CH2:15][S:14](=[O:17])[CH2:13][CH2:12]2)=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 225694274-(4-Nitrophenylmethyl)-thiomorpholine-1-oxide

생성물 1

HCID 225694714-(4-Aminophenylmethyl)-thiomorpholine-1-oxide

시약·촉매·용매 3

HCID 935Nickel촉매HCID 887Methanol용매HCID 6344Dichloromethane용매

실험 절차

1.2 g of Raney nickel are added to a solution of 3.9 g (15 mmol) of 4-(4-nitrophenylmethyl)-thiomorpholine-1-oxide in 10 ml of dichloromethane and 40 ml of methanol. The mixture is hydrogenated under a hydrogen atmosphere. The product is obtained by chromatography on silica gel (dichloromethane/methanol=9:1).

후처리

  1. customThe product is obtained by chromatography on silica gel (dichloromethane/methanol=9:1)

출처 및 근거

ORD 기록
ord-5100a5120f0944329eaaa65ceb44c7b3
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06855710B2

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