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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64422Generated: October 26, 2026

Water → tert-butyl (2E)-3-[2-(bromomethyl)-4-methylphenyl]acrylate

https://huagongshe.com/reaction/64422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-butyl (2E)-3-[2-(hydroxymethyl)-4-methylphenyl]acrylateHCID 86713430—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-butyl (2E)-3-[2-(bromomethyl)-4-methylphenyl]acrylateHCID 8671343193.9%

Reaction Steps

To a solution of 2.32 g of tert-butyl (2E)-3-[2-(hydroxymethyl)-4-methylphenyl]acrylate in 46 ml of THF were added 4.64 g of carbon tetrabromide and 3.67 g of triphenylphosphine under ice-cooling, followed by stirring at the same temperature for 2.5 hours. To the reaction mixture were added water and ethyl acetate to carry out a layer separation operation. The organic layer was washed with water and saturated brine in this order, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 2.73 g of tert-butyl (2E)-3-[2-(bromomethyl)-4-methylphenyl]acrylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447090B2
Source datasetuspto-grants-2016_09
ORD IDord-53f9abb562204188b258f4447111fcd2
Source noteuspto-grants-2016_09