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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656726Generated: November 3, 2026

Phenyl Bromoacetate → 2-Oxo-2-phenoxyethyl Lactate

https://huagongshe.com/reaction/1656726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl BromoacetateHCID 564919—
ReactantTetramethylammonium lactateHCID 21900266—
SolventDimethylformamideHCID 6228—
Product2-Oxo-2-phenoxyethyl LactateHCID 1901813231%

Reaction Steps

Phenyl bromoacetate (45.0 g, 0.209 mol) was added to a stirring solution of tetramethylammonium lactate (40.7 g of an 88% aq soln, 1.05 eq) in 50 mL of dimethylformamide at room temperature. The resulting tetramethylammonium bromide which separated from the reaction mixture as a solid was removed by filtration and washed with ethyl acetate. The dimethylformamide and ethyl acetate solutions were combined and washed with a NaHCO3 /brine solution, the separated aqueous phase was extracted with CH2Cl2, and the organic phases were combined and dried with MgSO4. The solvent was removed and the resulting residue was chromatographed on silica gel (ethyl acetate/hexane) to give the title compound (14.7 g, 31%): 1H NMR δ 1.50 (d, 3H, J=7.0), δ 3.12 (d, 1H, J=5.3), δ 4.40-4.49 (m, 1H), δ 4.87 (d, 1H, J=16.1), δ 4.99 (d, 1H, J=16.2), d 7.09-7.40 (5H, phenyl); HRMS calcd for C10H8O5TMS (M--CH3) 281.0845, obsd 281.0856.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254718
Source datasetuspto-grants-1993_10
ORD IDord-56e7c715b4ab4d31a6f587e64b370321
Source noteuspto-grants-1993_10