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

Ethanolamine → 2-chloro-5-beta-aminoethylamino-4-nitro-N-(beta-hydroxyethyl)aniline

HRID 4239
노트
인쇄 미리보기

반응식

HRID 4239 반응식
[Cl:1][C:2]1[C:11](Cl)=[CH:10][C:5]([NH:6][CH2:7][CH2:8][NH2:9])=[C:4]([N+:13]([O-:15])=[O:14])[CH:3]=1.[CH2:16]([CH2:18][NH2:19])[OH:17]>O>[Cl:1][C:2]1[CH:3]=[C:4]([N+:13]([O-:15])=[O:14])[C:5]([NH:6][CH2:7][CH2:8][NH2:9])=[CH:10][C:11]=1[NH:19][CH2:18][CH2:16][OH:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 700EthanolamineHCID 54360568N-(4,5-dichloro-2-nitrophenyl)ethane-1,2-diamine

생성물 1

HCID 541600842-chloro-5-beta-aminoethylamino-4-nitro-N-(beta-hydroxyethyl)aniline

시약·촉매·용매 1

HCID 962Water용매

실험 절차

0.04 mole (10 g) of 4,5-dichloro-2-nitro-N-β-aminoethylaniline prepared in the 1st stage is heated in 40 ml of monoethanolamine for 30 minutes to 100° C. The reaction mixture is diluted with 450 ml of iced water. An impurity is precipitated by adding hydrochloric acid and is removed by filtration. The filtrate is made alkaline with concentrated sodium hydroxide solution. The expected product precipitates. After filtration and drying, it is purified as its hydrochloride before being recrystallized from alcohol. It melts at 160° C.

후처리

  1. customAn impurity is precipitated
  2. additionby adding hydrochloric acid
  3. customis removed by filtration
  4. customThe expected product precipitates
  5. filtrationAfter filtration
  6. customdrying
  7. customit is purified as its hydrochloride
  8. custombefore being recrystallized from alcohol

출처 및 근거

ORD 기록
ord-4c54e3751d4842d7a5094d5ea6aa2e59
출처 데이터셋
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04725283

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트