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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509765Generated: October 30, 2026

Hydrochloric Acid → HCID 58444564, compound

https://huagongshe.com/reaction/1509765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantbismuth(III) bromideHCID 82232—
Reactant4-Bromo-3-fluorobenzaldehydeHCID 2783411—
Reactant2-ethylbut-3-en-1-olHCID 11159296—
SolventTolueneHCID 1140—
ProductHCID 58444564HCID 58444564—

Reaction Conditions

Temperature10 °C

Reaction Steps

72.9 g (0.16 mol) of bismuth(III) bromide are initially introduced in 50 ml of toluene at −10° C., and a solution of 50.0 g (0.25 mol) of 4-bromo-3-fluorobenzaldehyde in 250 ml of toluene is added dropwise. A solution of 27.0 g (0.27 mol) of 2-ethylbut-3-en-1-ol in 50 ml of toluene is metered in at this temperature, and the mixture is stirred at 10° C. for 2 h. Dilute hydrochloric acid is added to the batch, and the organic phase is separated off. The aqueous phase is extracted with toluene, and the combined organic phases are washed successively with water, saturated sodium hydrogen-carbonate solution and saturated sodium chloride solution. The solution is dried using sodium sulfate and concentrated to dryness. The crude product is purified by column chromatography (SiO2, n-heptane:toluene=2:1), giving 4-bromo-2-(4-bromo-3-fluorophenyl)-5-ethyltetrahydropyran as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211513B2
Source datasetuspto-grants-2012_07
ORD IDord-3d5c2e053fc14ce78b8460cad8562c14
Source noteuspto-grants-2012_07