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2-Fluorophenyl isocyanate → HCID 54351266, 화합물

HRID 435936
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HRID 435936 반응식
[CH3:1][NH:2][C:3]([NH:5][O:6][CH3:7])=[O:4].[F:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[N:15]=[C:16]=[O:17]>C1(C)C(C)=CC=CC=1>[CH3:1][NH:2][C:3]([N:5]([O:6][CH3:7])[C:16]([NH:15][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[F:8])=[O:17])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 855882-Fluorophenyl isocyanateHCID 2538391-methoxy-3-methylurea

생성물 1

HCID 54351266HCID 54351266, 화합물

시약·촉매·용매 1

HCID 7237O-Xylene용매2회

실험 절차

To 35 g (0.27 mol) of 1-methyl-3-methoxy urea in 150 ml xylene was added dropwise a solution of 37 g (0.27 mol) 2-fluorophenylisocyanate in 100 ml of xylene. The reaction mixture was refluxed for 4 hours. The reaction mixture was filtered while warm to remove a small amount of triethylamine hydrochloride (impurity in the urea reactant). The filtrate was evaporated to give the biuret product as a solid (m.p. 144°-147° C after recrystallization from benzene). Elemental analysis for fluorine showed: calc. 7.88%, found 7.64%.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. temperatureThe reaction mixture was refluxed for 4 hours
  2. filtrationThe reaction mixture was filtered
  3. temperaturewhile warm
  4. customto remove a small amount of triethylamine hydrochloride (impurity in the urea reactant)
  5. customThe filtrate was evaporated
  6. customto give
  7. customthe biuret product as a solid (m.p. 144°-147° C after recrystallization from benzene)

출처 및 근거

ORD 기록
ord-bf8f8915431d45f58f1697da2a3240a1
출처 데이터셋
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04007175

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