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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774431Generated: November 2, 2026

Benzyl Alcohol → Ethyl 2-(benzyloxy)acetate

https://huagongshe.com/reaction/1774431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductEthyl 2-(benzyloxy)acetateHCID 290299—

Reaction Steps

To a suspension of sodium hydride (44.2 g, 60 percent in oil, 1.1 mol) in dry toluene (800 mL) was added dropwise a solution of benzyl alcohol (108 mL, 1.0 mol, in 200 mL of toluene) at 0° C. under nitrogen over 30 min. The resulting mixture was stirred for 3.5 h at rt. The reaction was then cooled with ice water, to which a solution of ethyl bromoacetate (167.6 g, 1.0 mmol, in 200 mL of toluene) was added in 30 min and the resulting mixture was stirred for additional 25 min at 0° C. The reaction mixture was then poured into a mixed solution of 800 mL of cold water and 10 mL of cone HCl, followed by extraction with toluene. The organic layer was washed with saturated aq NaCl and dried over anhydrous MgSO4. Filtration, evaporation, and purification by flash chromatography provided ethyl(benzyloxy)acetate. (98 g, 50.5%). 1H-NMR δ (400 MHz, CDC3): 7.38-7.30 (m, 5H), 4.63 (s, 2H), 4.22 (q, J=7.2 Hz, 2H), 4.09 (s, 2H), 1.28 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260413B2
Source datasetuspto-grants-2016_02
ORD IDord-0dc215b8bcf544558ae12e65e853090f
Source noteuspto-grants-2016_02