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3-Chloro-2-methylaniline → N-(3-Chloro-2-methylphenyl)-3-nitropyridin-2-amine

HRID 614333
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HRID 614333 반응식
Cl[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[Cl:11][C:12]1[C:13]([CH3:19])=[C:14]([CH:16]=[CH:17][CH:18]=1)[NH2:15]>>[Cl:11][C:12]1[C:13]([CH3:19])=[C:14]([CH:16]=[CH:17][CH:18]=1)[NH:15][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 68943-Chloro-2-methylanilineHCID 796132-Chloro-3-nitropyridine

생성물 1

HCID 12445357N-(3-Chloro-2-methylphenyl)-3-nitropyridin-2-amine

반응 조건

온도
50 °C

실험 절차

A mixture of 6.3 g. (0.04 mole) of 2-chloro-3-nitropyridine and 16.9 g. (0.12 mole) of 3-chloro-2-methylaniline was heated in an oil bath to 170° C. when the temperature spontaneously rose to 185° C. After an additional 10 minutes at 180° C., the mixture was cooled to 50° C. and extracted with a solution of 75 ml. of water and 25 ml. of acetic acid. The insolubles were collected, air dried, dissolved in methylene chloride, and the solution was dried over magnesium sulfate. The solution was concentrated to a small volume and diluted with 50 ml. of ether which caused crystallization of 6.6 g. of 2-(3-chloro-2-methylanilino)-3-nitropyridine, m.p. 134°-135° C.

후처리

  1. additionA mixture of 6.3 g
  2. customspontaneously rose to 185° C
  3. extractionextracted with a solution of 75 ml
  4. customThe insolubles were collected
  5. customair dried
  6. dissolutiondissolved in methylene chloride
  7. dry with materialthe solution was dried over magnesium sulfate
  8. concentrationThe solution was concentrated to a small volume
  9. additiondiluted with 50 ml
  10. customcrystallization of 6.6 g

출처 및 근거

ORD 기록
ord-e2712bac3eaf4fe58e6e3246ef394e06
출처 데이터셋
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04144341

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