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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475849Generated: October 26, 2026

Ethanol → Ethyl 2-amino-2-(4-fluorophenyl)acetate

https://huagongshe.com/reaction/475849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
Reactant(1)-4-FluorophenylglycineHCID 98313—
ProductEthyl 2-amino-2-(4-fluorophenyl)acetateHCID 517841965%

Reaction Steps

To a cooled solution of 2-amino-2-(4-fluorophenyl)acetic acid (1.0 g, 6.17 mmol) in ethanol was added con. H2SO4 (1 mL) over a period of 1 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 (20 mL). The organic solution was washed with aqueous saturated NaHCO3 (15 mL×2), water (20 mL), brine solution (10 mL), dried over anhydrous Na2SO4 and evaporated under reduced pressure to give ethyl 2-amino-2-(4-fluorophenyl)acetate (0.75 g, 65%) as crude compound (oily liquid). The crude compound was taken to the next step without further purification. LC-MS (M+H2O)+=198.0. 1H NMR (400 MHz, DMSO-d6): δ 7.44-7.40 (2H, m), 7.18-7.13 (2H, m), 4.51 (1H, s), 4.12-4.01 (2H, m), 2.26 (2H, s), 1.12 (3H, t, J=8.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637525B2
Source datasetuspto-grants-2014_01
ORD IDord-acfa3a6638514255ac1823facbdf58da
Source noteuspto-grants-2014_01