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Ethanolamine → 3-Bromo-5-(2'-hydroxyethyl)amino-1-methyl-4-nitropyrazole

HRID 1376879
노트
인쇄 미리보기

반응식

HRID 1376879 반응식
[Br:1][C:2]1[C:6]([N+:7]([O-:9])=[O:8])=[C:5](Br)[N:4]([CH3:11])[N:3]=1.[CH2:12]([CH2:14][NH2:15])[OH:13].O>C(O)C>[Br:1][C:2]1[C:6]([N+:7]([O-:9])=[O:8])=[C:5]([NH:15][CH2:14][CH2:12][OH:13])[N:4]([CH3:11])[N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 700EthanolamineHCID 962WaterHCID 229186383,5-Dibromo-1-methyl-4-nitro-1H-pyrazole

생성물 1

HCID 229186243-Bromo-5-(2'-hydroxyethyl)amino-1-methyl-4-nitropyrazole수율 81%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
5 °C

실험 절차

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

3 g (10.5 mmoles) of 3,5-dibromo-1-methyl-4-nitropyrazole are heated in a solution of 30 ml ethanolamine in 30 ml ethanol for 15 hours at boiling temperature. The reaction mixture is then poured on 200 ml water, the separated product is filtered, washed with water (20 ml) and vacuum dried. Additional product crystallizes from the filtrate when cooled (5° C.). 2.25 g (81 percent of theory) of 3-bromo-5-(2'-hydroxyethyl)amino-1-methyl-4-nitropyrazole are obtained in the form of yellow crystals with a melting point of 150° C.

후처리

  1. filtrationthe separated product is filtered
  2. washwashed with water (20 ml) and vacuum
  3. customdried
  4. customAdditional product crystallizes from the filtrate when

출처 및 근거

ORD 기록
ord-934f0c9189c9415c8e6bfb115232ee5b
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05663366

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