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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2,4-difluorobenzeneHCID 67674—
Reactant1-Bromo-3,4,5-trifluorobenzeneHCID 611409—
Reactant3-(3,4,5-Trifluorophenyl)thiopheneHCID 23295528—
Product3(2,4-Difluorophenyl)thiopheneHCID 2274369297%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733683
Source datasetuspto-grants-1998_03
ORD IDord-84962d33083243bb8070accd1465b529
Source noteuspto-grants-1998_03