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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639127Generated: October 26, 2026

Hydrochloric Acid → Methyl 2-(4-bromostyryl)benzoate

https://huagongshe.com/reaction/1639127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant4-BromobenzaldehydeHCID 70741—
Reactant{[2-(Methoxycarbonyl)phenyl]methyl}(triphenyl)phosphanium bromideHCID 10743695—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(4-bromostyryl)benzoateHCID 5378636855.1%

Reaction Steps

In 1.0 liter of tetrahydrofuran was suspended 60 g of (2-methoxycarbonylbenzyl)triphenylphosphonium bromide and, 3.2 g of sodium hydride was added to the suspension followed by stirring at room temperature for 3 hours. Then, 18 g of 4-bromobenzaldehyde was added and the mixture was stirred at room temperature for 2 hours. After completion of the reaction, 500 ml of water, 200 ml of methanol and 100 ml of 0.1N hydrochloric acid aqueous solution were added thereto and the solvent was distilled off under reduced pressure. The residue was extracted with 500 ml of ethyl acetate. After washing in sequence with saturated sodium bicarbonate aqueous solution and then with saturated sodium chloride aqueous solution, the extract was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The resulting residue was recrystallized from methanol to give 17 g of methyl 2-(4-bromostyryl)benzoate as white needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882351
Source datasetuspto-grants-1989_11
ORD IDord-bf135495c06f4b528dd52a5be0a19f06
Source noteuspto-grants-1989_11