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Isopropylamine → N-Isopropyl-4-nitro-2-(trifluoromethyl)aniline

HRID 1863142
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인쇄 미리보기

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HRID 1863142 반응식
[F:1][C:2]([F:14])([F:13])[C:3]1[CH:4]=[C:5]([N+:10]([O-:12])=[O:11])[CH:6]=[CH:7][C:8]=1Cl.[CH:15]([NH2:18])([CH3:17])[CH3:16]>CS(C)=O>[CH:15]([NH:18][C:8]1[CH:7]=[CH:6][C:5]([N+:10]([O-:12])=[O:11])=[CH:4][C:3]=1[C:2]([F:14])([F:13])[F:1])([CH3:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6363IsopropylamineHCID 612132-Chloro-5-nitrobenzotrifluoride

생성물 1

HCID 20392080N-Isopropyl-4-nitro-2-(trifluoromethyl)aniline수율 100.2%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

To a solution of 45 g of 3-(trifluoromethyl)-4-chloronitrobenzene in 150 ml of DMSO was added 13 g of isopropylamine. The mixture was heated at 80°-90° C. for two hours, poured over ice water, acidified and filtered. The filter cake was dried to yield 49.6 g of product; m.p. 35°-36° C.

후처리

  1. temperatureThe mixture was heated at 80°-90° C. for two hours
  2. filtrationfiltered
  3. customThe filter cake was dried

출처 및 근거

ORD 기록
ord-53e8b43e3737455abc120b80728ee359
출처 데이터셋
uspto-grants-1979_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04168153

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