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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1,2,4-Trichlorobenzene → 1,3-Isobenzofurandione, 5-fluoro-

HRID 462821
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인쇄 미리보기

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HRID 462821 반응식
[F:1][C:2]1(F)[CH2:12][CH2:11][CH:5]2[C:6]([O:8][C:9](=[O:10])[CH:4]2[CH2:3]1)=[O:7].ClC1C=CC(Cl)=CC=1Cl>[Pd]>[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[O:10])[O:8][C:6](=[O:7])[C:5]2=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 131,2,4-TrichlorobenzeneHCID 140082491,3-Isobenzofurandione, 5,5-difluorohexahydro-

생성물 1

HCID 675721,3-Isobenzofurandione, 5-fluoro-수율 25%

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

A mixture of 50.0 parts of 4,4-difluorohexahydrophthalic anhydride and 10 parts of 5 percent palladium of carbon (Pd/C) catalyst in 578 parts of 1,2,4-trichlorobenzene was heated to reflux conditions and maintained at reflux for about 16 hours, with stirring. The reaction mixture was then cooled to about room temperature. Analysis of the reaction product using gas chromatographic techniques, indicated a yield of about 25 percent of 4-fluorophthalic anhydride, based on the difluorohexahydrophthalic anhydride reactant.

후처리

  1. temperaturewas heated
  2. temperatureto reflux conditions
  3. temperaturemaintained
  4. temperatureat reflux for about 16 hours
  5. temperatureThe reaction mixture was then cooled to about room temperature

출처 및 근거

ORD 기록
ord-c68a104204e6427b98c520213301f31e
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04517372

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