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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859941Generated: October 31, 2026

Benzyl Bromide → 3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl ester

https://huagongshe.com/reaction/1859941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl p-hydroxyphenyllactateHCID 21930973—
Product3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl esterHCID 1518615396.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

Benzyl bromide (21.9 g) and potassium carbonate (35.3 g) were added to a solution of ethyl 3-(4-hydroxyphenyl)lactate (22.4 g) in dimethylformnamide (220 ml). The mixture was stirred at 50° C. for 2 hours. The reaction mixture was partitioned between ethyl acetate and water. The ethyl acetate layer was separated and dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified via chromatography silica gel column using hexane/ethyl acetate=7/3 as the eluant to give the desired compound (31.0 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528525B1
Source datasetuspto-grants-2003_03
ORD IDord-be8c11a1835a486585b5db781b7789e0
Source noteuspto-grants-2003_03