홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

N-(3,4-dichlorobenzyl)-2-nitrobenzenesulfonamide → 2-amino-N-(3,4-dichlorobenzyl)benzenesulfonamide

HRID 569803
노트
인쇄 미리보기

반응식

HRID 569803 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:19]=[CH:20][C:21]=1[Cl:22])[CH2:5][NH:6][S:7]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[N+:16]([O-])=O)(=[O:9])=[O:8]>C(O)(=O)C.[Fe]>[NH2:16][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[S:7]([NH:6][CH2:5][C:4]1[CH:19]=[CH:20][C:21]([Cl:22])=[C:2]([Cl:1])[CH:3]=1)(=[O:9])=[O:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 1000717N-(3,4-dichlorobenzyl)-2-nitrobenzenesulfonamide

생성물 1

HCID 37280272-amino-N-(3,4-dichlorobenzyl)benzenesulfonamide수율 92.7%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 176Acetic Acid용매

반응 조건

온도
100 °C

실험 절차

A mixture of N-(3,4-dichlorobenzyl)-2-nitrobenzenesulfonamide (4 g) and iron (2 g) in acetic acid (30 ml) was stirred at 100° C. for 45 minutes. After cooling, the iron was filtered off. The filtrate was made alkaline with a diluted aqueous sodium hydroxide and extracted with ethyl acetate. The extract was washed with water, dried and evaporated. Recrystallization from ethyl ether gave 2-amino-N-(3,4-dichlorobenzyl)benzenesulfonamide (3.40 g).

후처리

  1. temperatureAfter cooling
  2. filtrationthe iron was filtered off
  3. extractionextracted with ethyl acetate
  4. washThe extract was washed with water
  5. customdried
  6. customevaporated
  7. customRecrystallization from ethyl ether

출처 및 근거

ORD 기록
ord-bb18963c1b3f4082bd9183a4a7b60aaa
출처 데이터셋
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04734419

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트