HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280727Generated: October 29, 2026
Sulfolane → Benzene, 1-chloro-2,3-difluoro-5-(trifluoromethyl)-
https://huagongshe.com/reaction/280727
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfolane | HCID 31347 | — |
| Reactant | Benzene, 1,3-dichloro-2-fluoro-5-(trifluoromethyl)- | HCID 157026 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Product | Benzene, 1-chloro-2,3-difluoro-5-(trifluoromethyl)- | HCID 2736496 | — |
Reaction Steps
A mixture of 55 parts of anhydrous potassium fluoride and 45.32 parts of 3,5-dichloro-4-fluorobenzotrifluoride in 291 parts of sulfolane was heated and maintained at about 216° to 256° for a period of about 55 hours, while product vapors were removed through a distillation column at a head temperature of about 130°-150° C. A total of 32.02 parts of distillate was collected and analyzed by gas chromatography/mass spectrometry. The distillate was found to be 25.1 percent 3,5-dichloro-4-fluorobenzotrifluoride; 65.9 percent 3-chloro-4,5-difluorobenzotrifluoride; 8.6 percent 3,4,5-trifluorobenzotrifluoride and trace amounts of 4-chloro-3,5-difluorobenzotrifluoride. The desired 3-chloro-4,5-difluorobenzotrifluoride was isolated by distillation (b.p. 122° C.) to recover it in essentially pure form (greater than 99 percent pure). The 3,5-dichloro-4-fluoro isomer is recycled.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04590315 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-c6787f22a7ef4c1083fa9abc315968bb |
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| Source note | uspto-grants-1986_05 |
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