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Phosgene → 2,6-Diethyl-4-nitrophenylisocyanate

HRID 26024
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인쇄 미리보기

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HRID 26024 반응식
[C:1](Cl)(Cl)=[O:2].[CH2:5]([C:7]1[CH:13]=[C:12]([N+:14]([O-:16])=[O:15])[CH:11]=[C:10]([CH2:17][CH3:18])[C:8]=1[NH2:9])[CH3:6]>C1(C)C=CC=CC=1>[CH2:17]([C:10]1[CH:11]=[C:12]([N+:14]([O-:16])=[O:15])[CH:13]=[C:7]([CH2:5][CH3:6])[C:8]=1[N:9]=[C:1]=[O:2])[CH3:18]
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참가 물질

4

반응물 2

HCID 6371PhosgeneHCID 81426772,6-Diethyl-4-nitroaniline

생성물 1

HCID 203836312,6-Diethyl-4-nitrophenylisocyanate

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

Excess phosgene is bubbled into a warm solution of 21.5 g (0.11 moles) of 2,6-diethyl-4-nitroaniline in toluene (250 ml). After the addition, the mixture is heated to reflux and approximately 200 ml of toluene are distilled. The remainder of the toluene is removed under vacuum and the remaining brown semi-solid is distilled under vacuum to give 2,6-diethyl-4-nitrophenylisocyanate, b.p. 135°-144° C./1 mm, as a yellow liquid which crystallized on standing.

후처리

  1. additionAfter the addition
  2. temperaturethe mixture is heated
  3. temperatureto reflux
  4. distillationapproximately 200 ml of toluene are distilled
  5. customThe remainder of the toluene is removed under vacuum
  6. distillationthe remaining brown semi-solid is distilled under vacuum

출처 및 근거

ORD 기록
ord-f7fe7bcfb4234004b8032086d9231bf4
출처 데이터셋
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04147804

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