HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370153Generated: October 25, 2026
Ethanol → Ethyl 2-(4-fluorophenyl)-2-hydroxyacetate
https://huagongshe.com/reaction/2370153
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Fluoromandelic acid | HCID 98068 | — |
| Product | Ethyl 2-(4-fluorophenyl)-2-hydroxyacetate | HCID 111010 | 90% |
Reaction Steps
To a cooled solution of 2-(4-fluorophenyl)-2-hydroxyacetic acid (5.0 g, 29.4 mmol) in ethanol was added con. H2SO4 (10 mL) over a period of 10 min. The reaction mixture was heated at reflux for 5 h. The solvent was evaporated under reduced pressure and the residue was diluted with ethyl acetate (25 mL). The organic solution was washed with aqueous saturated NaHCO3 (25 mL×2), water (20 mL), brine solution (10 mL), dried over anhydrous Na2SO4 and evaporated under reduced pressure to give ethyl 2-(4-fluorophenyl)-2-hydroxyacetate (5.0 g, 90%) as crude compound (oily liquid). The crude compound was taken to the next step without further purification. LC-MS (M+H2O)+=216. 1H NMR (400 MHz, DMSO-d6): δ 7.43-7.46 (2H, m), 7.17-7.20 (2H, m), 6.11-6.13 (1H, m), 5.14 (1H, d, J=5.20 Hz), 3.35-4.13 (2H, m), 1.12-1.15 (3H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710061B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-2683c2af536545ec82bf611299794690 |
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| Source note | uspto-grants-2014_04 |
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