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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Acid → 1-(2-Ureidoethylamino)-4-nitrobenzene

HRID 436330
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인쇄 미리보기

반응식

HRID 436330 반응식
[NH2:1][CH2:2][CH2:3][NH:4][C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][CH:6]=1.C(O)(=O)C.[N-:18]=[C:19]=[O:20].[K+]>O>[NH:1]([CH2:2][CH2:3][NH:4][C:5]1[CH:6]=[CH:7][C:8]([N+:11]([O-:13])=[O:12])=[CH:9][CH:10]=1)[C:19]([NH2:18])=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 236318N-(2-aminoethyl)-N-(4-nitrophenyl)amineHCID 11051572Potassio isocyanate

생성물 1

HCID 73423441-(2-Ureidoethylamino)-4-nitrobenzene수율 73.6%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

37 g (0.2 mole) of para-[N-(β-amino-ethyl)]amino nitrobenzene is dissolved in 200 cm3 of water at 30° C, to which 15 cm3 (0.26 mole) of acetic acid had been added. 17 g (0.21 mole) of potassium isocyanate is then rapidly added. The desired product precipitates immediately in a form which is very difficult to dry. 150 cm3 of acetic acid is added to the reaction mixture and it is heated until the urein is completely dissolved. After slow cooling, drying yields 33 g of para-[N-(β-ureidoethyl)]amino nitrobenzene in a well crystallized form, which is practically prue and melts at 187° C.

후처리

  1. additionhad been added
  2. customThe desired product precipitates immediately in a form which
  3. customto dry
  4. addition150 cm3 of acetic acid is added to the reaction mixture and it
  5. temperatureis heated until the urein
  6. dissolutionis completely dissolved
  7. customAfter slow cooling, drying

출처 및 근거

ORD 기록
ord-38e11ac44724494e9dbb52653c6ae6b1
출처 데이터셋
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04008272

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