HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3076Generated: October 25, 2026
1-Bromo-2,4-difluorobenzene → 3(2,4-Difluorophenyl)thiophene
https://huagongshe.com/reaction/3076
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-2,4-difluorobenzene | HCID 67674 | — |
| Reactant | 1-Bromo-3,4,5-trifluorobenzene | HCID 611409 | — |
| Reactant | 3-(3,4,5-Trifluorophenyl)thiophene | HCID 23295528 | — |
| Product | 3(2,4-Difluorophenyl)thiophene | HCID 22743692 | 97% |
Reaction Steps
The same procedures set forth above in Example (1)(a) for synthesizing 3(3,4,5-trifluorophenyl)thiophene were followed, with the exception that 1-bromo-2,4-difluorobenzene was substituted for 1-bromo-3,4,5-trifluorobenzene as the 1-bromo-substituted fluorobenzene, and the coupling reaction mixture was heated to reflux in an oil bath for 10 hours with stirring at 80° C. (as opposed to being heated in an oil bath for 0.5 hour with periodically stirring). No further purification by recrystallization was required to obtain a 97 to 98% pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05733683 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-84962d33083243bb8070accd1465b529 |
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| Source note | uspto-grants-1998_03 |
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