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Ethylenediamine → [2-(2-Aminoethyl)amino-5-nitrophenyl]-benzyl sulphone

HRID 978636
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인쇄 미리보기

반응식

HRID 978636 반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11]([CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)(=[O:13])=[O:12].[NH2:21][CH2:22][CH2:23][NH2:24]>C(O)(C)C>[NH2:21][CH2:22][CH2:23][NH:24][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11]([CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)(=[O:13])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3301EthylenediamineHCID 20203466Benzyl 2-chloro-5-nitrophenyl sulphone

생성물 1

HCID 20203455[2-(2-Aminoethyl)amino-5-nitrophenyl]-benzyl sulphone

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

16.0 g of benzyl 2-chloro-5-nitrophenyl sulphone and 12.0 g of 1,2-diaminoethane are refluxed in 100 ml of isopropanol for one hour. The reaction mixture is cooled down, and the solids are filtered off with suction, are washed with 50 ml of water and are dried. This gives 19.2 g of pale yellow [2-(2-aminoethyl)-amino-5-nitrophenyl]-benzyl sulphone.

후처리

  1. temperatureThe reaction mixture is cooled down
  2. filtrationthe solids are filtered off with suction
  3. washare washed with 50 ml of water
  4. customare dried

출처 및 근거

ORD 기록
ord-28f4c20163274bfca27c1b341a9c0202
출처 데이터셋
uspto-grants-1987_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04665179

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