Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532793Generated: October 30, 2026

Tetrahydrofuran → Methyl 2-(4-chlorophenyl)-3-(2,2,2-trifluoroethylamino)propanoate

https://huagongshe.com/reaction/532793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 3-amino-2-(4-chlorophenyl)propanoate hydrochlorideHCID 66617900—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(4-chlorophenyl)-3-(2,2,2-trifluoroethylamino)propanoateHCID 6661799393%

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 was 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853199B2
Source datasetuspto-grants-2014_10
ORD IDord-3b7bac2a667d442299097108052d51e9
Source noteuspto-grants-2014_10