HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491552Generated: October 31, 2026
Phenyl Bromoacetate → 2-Oxo-2-phenoxyethyl Lactate
https://huagongshe.com/reaction/1491552
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl Bromoacetate | HCID 564919 | — |
| Reactant | Tetramethylammonium lactate | HCID 21900266 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Oxo-2-phenoxyethyl Lactate | HCID 19018132 | 31% |
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 δ1.50 (d, 3H, J=7.0), δ3.12 (d, 1H, J=5.3), δ4.40-4.49 (m, 1H), δ4.87 (d, 1H, J=16.1), δ4.99 (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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05371001 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-3b66eb9a16df45a1ae467392d45a747e |
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| Source note | uspto-grants-1994_12 |
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