HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451134Generated: October 25, 2026
Ethanol → Ethyl 2-amino-2-(4-fluorophenyl)acetate
https://huagongshe.com/reaction/451134
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | (1)-4-Fluorophenylglycine | HCID 98313 | — |
| Product | Ethyl 2-amino-2-(4-fluorophenyl)acetate | HCID 5178419 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486952B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-81f39d8a563d41ffb36613701093d848 |
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| Source note | uspto-grants-2013_07 |
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