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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948508Generated: October 31, 2026

Tributylphosphine → HCID 66955245, compound

https://huagongshe.com/reaction/1948508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
ReactantCesium fluorideHCID 25953—
ReactantTributylvinyltinHCID 81998—
ReactantPotassium FluorideHCID 522689—
Reactant4-Bromo-2-(trifluoromethyl)benzonitrileHCID 22337825—
CatalystHexaneHCID 8058—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 66955245HCID 66955245—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 4-bromo-2-(trifluoromethyl)benzonitrile (500 mg, 2.000 mmol), cesium fluoride (668 mg, 4.40 mmol), tri-n-butylphosphine in hexane (0.347 mL, 0.120 mmol) and Pd2(dba)3 (36.6 mg, 0.040 mmol) in toluene (10 mL) was added tributyl(vinyl)stannane (0.587 mL, 2.000 mmol). The reaction mixture was heated at 80° C. overnight. Next, saturated KF solution was added and the resulting mixture was stirred 1 hour and then filtered. The filtrate was diluted with ethyl acetate and washed with H2O. The organic layer was dried with MgSO4, filtered, and concentrated. The solids were purified on a silica gel cartridge using an EtOAc/hexanes gradient to yield 450 mg of 2-(trifluoromethyl)-4-vinylbenzonitrile. 1H NMR (400 MHz, chloroform-d) δ ppm 7.79 (1H, s), 7.67 (1H, dd, J=7.91, 1.76 Hz), 7.40-7.45 (1H, m), 6.77 (1H, dd, J=17.58, 10.99 Hz), 5.97 (1H, d, J=17.58 Hz), 5.58 (1H, d, J=10.99 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399451B2
Source datasetuspto-grants-2013_03
ORD IDord-e264196197834eacbf75044cde6a94e1
Source noteuspto-grants-2013_03