HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559457Generated: October 30, 2026
Tetrahydrofuran → Methyl 2-(4-chlorophenyl)-3-(2,2,2-trifluoroethylamino)propanoate
https://huagongshe.com/reaction/559457
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2,2,2-Trifluoroethyl trifluoromethanesulfonate | HCID 80366 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 3-amino-2-(4-chlorophenyl)propanoate hydrochloride | HCID 66617900 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(4-chlorophenyl)-3-(2,2,2-trifluoroethylamino)propanoate | HCID 66617993 | 93% |
Reaction Steps
A solution of methyl 3-amino-2-(4-chlorophenyl)propanoate hydrochloride (215 mg, 0.86 mmol) in 1:1 THF:DMF (3.0 mL) was treated with DIEA (389 uL, 2.23 mmol) at room temperature. Trifluoroethyl triflate (299 mg, 1.29 mmol) was added to the mixture, and the reaction was stirred for 20 hours to completion. The mixture was partitioned between ethyl acetate and diluted NaHCO3 solution. The aqueous portion was extracted twice, and the combined organic portions were washed with water (3×). The organic portion washed with brine, separated, dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by chromatography (silica gel eluted with 4:1 hexanes:ethyl acetate, Rf=0.18) to afford the pure methyl 2-(4-chlorophenyl)-3-(2,2,2-trifluoroethylamino)propanoate (235 mg, 93%) as a colorless oil. LCMS (APCI+) m/z 296.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08063050B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-db65ff4fd2434e6e9458769583b8c395 |
|---|
| Source note | uspto-grants-2011_11 |
|---|