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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037079Generated: October 30, 2026

Cesium carbonate → 1,3-Dichloro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene

https://huagongshe.com/reaction/1037079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1-Propene, 2-bromo-3,3,3-trifluoro-HCID 272696—
Reactant3,5-Dichlorophenylboronic acidHCID 2734331—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product1,3-Dichloro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzeneHCID 2315982380%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 3,5-dichlorophenylboronic acid (3.8 g, 20.0 mmol), 2-bromo-3,3,3-trifluoro-prop-1-ene (4.9 g, 28 mmol), Cs2CO3 (20 mL, 2 M, 40 mmol) and Pd(PPh3)2Cl2 (421 mg) in THF (30 mL) was heated at 70° C. in a sealed tube for 4 h. The mixture was cooled to rt and partitioned between ether and H2O. The aqueous layer was extracted with EA and the combined organic layers were dried over Na2SO4. The solvent was removed under reduced pressure and the crude product was purified by column chromatography over silica gel eluted with hexanes to give 1,3-dichloro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene (3.85 g; yield 80%). 1H NMR (500 MHz, CDCl3): δ 7.41 (s, 1H), 7.35 (s, 2H), 6.06 (s, 1 H), 5.83 (s, 1 H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546357B2
Source datasetuspto-grants-2013_10
ORD IDord-2719f458349b478aba08f382bdefd33e
Source noteuspto-grants-2013_10