Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194740Generated: October 31, 2026

Sodium hydride → 2-(2,2,2-Trifluoro-ethyl)-malonic acid dibenzyl ester

https://huagongshe.com/reaction/2194740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
ReactantDibenzyl malonateHCID 84754—
SolventTetrahydrofuranHCID 8028—
Product2-(2,2,2-Trifluoro-ethyl)-malonic acid dibenzyl esterHCID 6705048868%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of 60% sodium hydride (0.678 g, 16.97 mmol) in THF (100 mL) at room temperature was added malonic acid dibenzyl ester (4.825 g, 16.97 mmol) to give a clear solution after 30 min. Trifluoro-methanesulfonic acid 2,2,2-trifluoro-ethyl ester (3.52 g, 15.43 mmol) was added and reaction mixture was stirred at 50° C. for 48 h. The reaction mixture was concentrated, partioned between ethyl ether and washed with saturated ammonium chloride solution and acidified with 1N HCl. The mixture was extracted with ethyl ether (2×), dried (MgSO4), and concentrated. The resulting residue was purified by flash column chromatography (silica gel, 0 to 0% ethyl ether/hexanes) to give a colorless oil (3.844 g, 68%). 1H NMR (300 MHz, CDCl3): δ 7.4-7.2 (m, 10H), 5.15 (s, 4H), 3.75 (t, J=6.9 Hz, 1H), 2.9-7.7 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334295B2
Source datasetuspto-grants-2012_12
ORD IDord-292d7016cbf04211ab1d980b67dc5fe0
Source noteuspto-grants-2012_12