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2,5-Dichloronitrobenzene → 4-Chloro-N-[(4-chlorophenyl)methyl]-2-nitroaniline

HRID 893345
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인쇄 미리보기

반응식

HRID 893345 반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10].[Cl:12][C:13]1[CH:20]=[CH:19][C:16]([CH2:17][NH2:18])=[CH:15][CH:14]=1>O>[Cl:12][C:13]1[CH:20]=[CH:19][C:16]([CH2:17][NH:18][C:2]2[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=2[N+:9]([O-:11])=[O:10])=[CH:15][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 69772,5-DichloronitrobenzeneHCID 660364-Chlorobenzylamine

생성물 1

HCID 149529774-Chloro-N-[(4-chlorophenyl)methyl]-2-nitroaniline수율 57.6%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

25 g of 2,5-dichloronitrobenzene and 36.9 g of 4-chlorobenzylamine are heated for two hours at 135° C., it being necessary for the temperature always to be kept below 140° C. After cooling, the mixture is taken up with water and extracted with ethyl acetate. After drying over magnesium sulfate and evaporation under vacuum, the residue is taken up with ether and the crystals obtained are filtered off and washed with ether to give 22.3 g of 2-(4-chlorophenylmethylamino)-5-chloronitrobenzene in the form of crystals melting at 120° C.

후처리

  1. customto be kept below 140° C
  2. temperatureAfter cooling
  3. extractionextracted with ethyl acetate
  4. dry with materialAfter drying over magnesium sulfate and evaporation under vacuum
  5. customthe crystals obtained
  6. filtrationare filtered off
  7. washwashed with ether

출처 및 근거

ORD 기록
ord-5ab13f76a8a94b68abb4500fd2be9b32
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05124336

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