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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921875Generated: October 26, 2026

Carbon tetrabromide → 3,5-Difluoro-4-triisopropylsilanyloxybenzyl bromide

https://huagongshe.com/reaction/1921875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant1,3-Difluoro-5-hydroxymethyl-2-triisopropylsilanyloxybenzeneHCID 57971896—
SolventDichloromethaneHCID 6344—
Product3,5-Difluoro-4-triisopropylsilanyloxybenzyl bromideHCID 57971946—

Reaction Conditions

Temperature0 °C

Reaction Steps

7.40 g (23.4 mmol) of 1,3-difluoro-5-hydroxymethyl-2-triisopropylsilanyloxybenzene are dissolved in 90 ml of dry dichloromethane by stirring at 0° C. under argon. 10.1 g (30.4 mmol) of tetrabromomethane and 7.97 g (30.4 mmol) of triphenylphosphine are successively added to this solution, and the mixture is then stirred under reflux under argon for 12 h. The reaction mixture is washed with water, the organic phase is separated off, dried over magnesium sulfate and filtered, and the solvent is distilled out in vacuo. The oily residue is taken up in diethyl ether and stirred at RT, then filtered, and the filtrate is concentrated. Chromatography of the residue on silica gel 60 (mobile phase: cyclohexane/ethyl acetate 9:1) results in 7.42 g (15.6 mmol, 84% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173704B2
Source datasetuspto-grants-2012_05
ORD IDord-2aa110eae3014579aa1cd98e37f48bf7
Source noteuspto-grants-2012_05