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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371287Generated: October 30, 2026

Hydroxyphenylacetic acid → HCID 10882152, compound

https://huagongshe.com/reaction/2371287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyphenylacetic acidHCID 127—
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
SolventDimethylformamideHCID 6228—
ProductHCID 10882152HCID 10882152—

Reaction Steps

To a stirred solution of 4-hydroxy-phenyl acetic acid (10.0 g, 65.72 mmol) in DMF (70 mL) at rt were added Cs2CO3 (47.11 g, 144.5 mmol) and benzyl bromide (17.29 mL, 144.5 mmol). The reaction mixture was stirred overnight at room temperature, heated at 100° C. for 1 h and cooled to rt. The solvent was removed under reduced pressure and poured into H2O. The aqueous solution was extracted with ethyl acetate and the combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product was recrystallization in hexanes to afford (4-benzyloxy-phenyl)acetic acid benzyl ester as a yellow solid. (20.5 g, 94%): 1H NMR (300 MHz, CDCl3): δ 7.25-7.34 (m, 10H), 7.14 (d, J=8.4 Hz, 2H), 7.02 (d, J=8.4 Hz, 2H), 5.50 (s, 2H), 5.12 (s, 2H), 3.61 (s, 2H); TLC conditions: Uniplate silica gel, 250 microns; mobile phase=ethyl acetate-hexanes (1:5); Rf=0.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710236B2
Source datasetuspto-grants-2014_04
ORD IDord-3ee850882d89429b8c4126612eb87491
Source noteuspto-grants-2014_04