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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186314Generated: November 1, 2026

Benzyl Bromide → Benzyl 2-Benzylacrylate

https://huagongshe.com/reaction/2186314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Benzylacrylic AcidHCID 303571—
SolventDimethylformamideHCID 6228—
ProductBenzyl 2-BenzylacrylateHCID 1091201260.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

The title acid of Step 8 (5.2 g, 30 mmol) was dissolved in dimethylformamide (25 mL) and cooled to 0° C. To this potassium carbonate (5.7 g, 41.48 mmol) was added followed by benzyl bromide (5.7 g, 29.7 mmol). The mixture was stirred at room temperature overnight. The mixture was filtered and the filtrate was diluted with ethyl acetate, washed with 3 times of water, brine. The solution was dried (Na2SO4) and evaporated. The residue was purified by flash chromatography on silica gel, eluting with 90:10 heptane:ethyl acetate to give the pure title compound as yellow oil (4.5 g, 60% yield). 1H NMR: 300 MHz spectrum consistent with proposed structure. Anal: calcd. for C17H16O2: C, 80.93; H, 6.39. Found: C, 80.69; H, 6.47.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403648B2
Source datasetuspto-grants-2002_06
ORD IDord-1966dfad98c541f5abaeb9d5a8dbea54
Source noteuspto-grants-2002_06