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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

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 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 numberUS08063050B2
Source datasetuspto-grants-2011_11
ORD IDord-db65ff4fd2434e6e9458769583b8c395
Source noteuspto-grants-2011_11