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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241012Generated: October 26, 2026

Water → 1-Bromo-3-((4-(difluoromethoxy)phenyl)ethynyl)benzene

https://huagongshe.com/reaction/2241012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant1-(Difluoromethoxy)-4-iodobenzeneHCID 2737008—
Reactant1-Bromo-3-ethynylbenzeneHCID 11480818—
SolventEthyl AcetateHCID 8857—
Product1-Bromo-3-((4-(difluoromethoxy)phenyl)ethynyl)benzeneHCID 59790332—

Reaction Steps

To a mixture of 1-bromo-3-ethynylbenzene (9.1 g, 50.26 mmol), TEA (22.38 g, 30.8 mL, 221.1 mmol), PdCl2(ACN)2 (1.41 g, 2.01 mmol) and DMF (60 mL) was added 4-iodo(difluoromethoxy)benzene (10.85 g, 40.21 mmol). The reaction mixture became warm after the addition was completed. The mixture was stirred for 4 h. Then it was poured into water and diluted with EtOAc. The aqueous layer was separated and extracted twice with EtOAc. The combined organic layers were dried over Na2SO4, filtered, and concentrated onto 40 g Celite. Flash chromatography (SiO2, Hexanes) provided 12 g, 92%, of the title compound as a yellow oil that crystallized into a yellow solid upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723368B2
Source datasetuspto-grants-2010_05
ORD IDord-92121d58d1d94b39990c9a0300322426
Source noteuspto-grants-2010_05