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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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ethyl P-methyl-2-nitro-5-chlorophenylphosphinate → ethyl P-methyl-2-amino-5-chlorophenylphosphinate

HRID 463561
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인쇄 미리보기

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HRID 463561 반응식
[CH3:1][P:2]([C:7]1[CH:12]=[C:11]([Cl:13])[CH:10]=[CH:9][C:8]=1[N+:14]([O-])=O)(=[O:6])[O:3][CH2:4][CH3:5]>CO.[Pd]>[CH3:1][P:2]([C:7]1[CH:12]=[C:11]([Cl:13])[CH:10]=[CH:9][C:8]=1[NH2:14])(=[O:6])[O:3][CH2:4][CH3:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 53860251ethyl P-methyl-2-nitro-5-chlorophenylphosphinate

생성물 1

HCID 53901381ethyl P-methyl-2-amino-5-chlorophenylphosphinate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

Ethyl P-methyl-2-nitro-5-chlorophenylphosphinate (1.7 g, 7.5 mmol) dissolved in methanol (25 ml) is added to 200 mg of 5% palladium on carbon. The mixture is hydrogenated at 32 psi for 1 hour. The catalyst is then filtered off and the filtrate is evaporated to dryness to give ethyl P-methyl-2-amino-5-chlorophenylphosphinate.

후처리

  1. filtrationThe catalyst is then filtered off
  2. customthe filtrate is evaporated to dryness

출처 및 근거

ORD 기록
ord-0f90b9e8e3224c6c9f66c15bc4a19f4a
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04520197

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