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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453407Generated: October 30, 2026

Cesium fluoride → 5-Allyl-1,2-difluoro-3-methoxybenzene

https://huagongshe.com/reaction/453407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant5-Bromo-1,2-difluoro-3-methoxybenzeneHCID 2773288—
ReactantPinacolyl allylboronateHCID 86657601—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product5-Allyl-1,2-difluoro-3-methoxybenzeneHCID 55264893—

Reaction Steps

3.06 g of 1-bromo-3,4-difluoro-5-methoxybenzene (D2), 4.54 ml of pinacolyl allylboronate, 3.04 g of tetrakis(triphenylphosphine)palladium(0) and 7.62 g of caesium fluoride are suspended in 115 ml of tetrahydrofuran under an argon atmosphere. The reaction mixture is subsequently heated under reflux for 48 h. For work-up, the mixture is diluted with 400 ml of diethyl ether and extracted with 100 ml of water and 100 ml of saturated NaCl solution. The combined organic phases are dried over Na2SO4, filtered and evaporated to dryness in vacuo. The residue is purified by flash column chromatography on silica gel (solvent: cyclohexane), giving 1.59 g of the title compound as a colourless oil; MS: 184.0 (M+); TLC: Rf=0.69 (cyclohexane/ethyl acetate 8:1 parts by volume).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492440B2
Source datasetuspto-grants-2013_07
ORD IDord-ce6f1d4b78b64bd68343e439c71486af
Source noteuspto-grants-2013_07