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

HRID 462823
Notes
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Reaction equation

HRID 462823 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 23938PalladiumCatalyst

Procedure

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.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  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

Sources & evidence

ORD record
ord-40179c84082049ed9cdd852cdd4a12ac
Source dataset
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04517372

Reaction notes

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