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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Cyanoacetic acid → 2-Cyano-N-(2-methyl-6-nitrophenyl)acetamide

HRID 1161642
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인쇄 미리보기

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HRID 1161642 반응식
[CH3:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:5]([N+:9]([O-:11])=[O:10])[C:3]=1[NH2:4].[C:12]([CH2:14][C:15](O)=[O:16])#[N:13].P(Cl)(Cl)(Cl)(Cl)Cl>C1C=CC=CC=1>[C:12]([CH2:14][C:15]([NH:4][C:3]1[C:5]([N+:9]([O-:11])=[O:10])=[CH:6][CH:7]=[CH:8][C:2]=1[CH3:1])=[O:16])#[N:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 9740Cyanoacetic acidHCID 112982-Methyl-6-nitroanilineHCID 24819Phosphorus pentachloride

생성물 1

HCID 215049312-Cyano-N-(2-methyl-6-nitrophenyl)acetamide수율 66.3%

시약·촉매·용매 1

HCID 241Benzene용매

반응 조건

온도
60 °C

실험 절차

To a solution of 2-methyl-6-nitroaniline (25 g, 164.3 mmol) in benzene (200 ml) were added cyanoacetic acid (14.5 g, 170.46 mmol) and PCl5 (35 g, 168 mmol). The reaction mixture was heated at 60° C. for 7 h. After cooling to rt, the reaction mixture was filtered and the solid was washed with benzene and water. The solid was dried under reduced pressure to afford the title acetamide (24 g, 109 mmol) as a yellow solid.

후처리

  1. temperatureAfter cooling to rt
  2. filtrationthe reaction mixture was filtered
  3. washthe solid was washed with benzene and water
  4. customThe solid was dried under reduced pressure

출처 및 근거

ORD 기록
ord-42d3ef16dcdb4244ba01adc18e4ef5d6
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07820655B2

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