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Thiophosgene → 4-Cyano-2,5-difluoro-phenyl isothiocyanate

HRID 1250433
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HRID 1250433 반응식
[C:1]([C:3]1[C:9]([F:10])=[CH:8][C:6]([NH2:7])=[C:5]([F:11])[CH:4]=1)#[N:2].[C:12](Cl)(Cl)=[S:13]>C1(C)C=CC=CC=1>[C:1]([C:3]1[C:9]([F:10])=[CH:8][C:6]([N:7]=[C:12]=[S:13])=[C:5]([F:11])[CH:4]=1)#[N:2]
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참가 물질

4

반응물 2

HCID 10040ThiophosgeneHCID 27359004-Amino-2,5-difluorobenzonitrile

생성물 1

HCID 183261924-Cyano-2,5-difluoro-phenyl isothiocyanate

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

10.0 g (65 mmol) of 4-cyano-2,5-difluoro-aniline are introduced into 100 ml of toluene and 8.2 g (71 mmol) of thiophosgene are slowly added to the mixture heated to 80° C. to 90° C. The reaction mixture is then refluxed for approximately 40 hours. Then, after the solvent has been carefully distilled off under reduced pressure, the product (4-cyano-2,5-difluoro-phenyl isothiocyanate) is obtained as an ochre colourant.

후처리

  1. additionare slowly added to the mixture
  2. temperatureheated to 80° C. to 90° C
  3. temperatureThe reaction mixture is then refluxed for approximately 40 hours
  4. distillationThen, after the solvent has been carefully distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-ccbe2fe6b47046218ece3ff2a8b4e13e
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06339044B1

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