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2-Chlorotoluene → 1,3-Isobenzofurandione, 5-fluoro-

HRID 462823
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HRID 462823 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=CC=1C>[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
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참가 물질

4

반응물 2

HCID 72382-ChlorotolueneHCID 140082491,3-Isobenzofurandione, 5,5-difluorohexahydro-

생성물 1

HCID 675721,3-Isobenzofurandione, 5-fluoro-수율 37%

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

A mixture of 500 parts of 4,4-difluorohexahydrophthalic anhydride and 100 parts of 5 percent Pd/C catalyst in 3787 parts of o-chlorotoluene was charged to an autoclave reactor. The autoclave atmosphere was purged with nitrogen. The autoclave when then sealed, heated to 300°-350° and maintained thereat for about 3 hours, then cooled to about room temperature. Analysis of the reaction product, by gas chromatographic techniques indicated a 37 percent yield of 4-fluorophthalic anhydride, based on the difluorohexahydrophthalic anhydride reactant.

후처리

  1. additionwas charged to an autoclave reactor
  2. customThe autoclave atmosphere was purged with nitrogen
  3. customThe autoclave when then sealed
  4. temperatureheated to 300°-350°
  5. temperaturemaintained
  6. temperaturecooled to about room temperature

출처 및 근거

ORD 기록
ord-40179c84082049ed9cdd852cdd4a12ac
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04517372

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