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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8474Generated: October 25, 2026

Water → Diethyl [2,3,4-trifluoro[(1S)-2-hydroxy-1-methylethyl]anilino]methylenemalonate

https://huagongshe.com/reaction/8474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
ReactantPotassium HydroxideHCID 14797—
Reactant(2S)-2-(2,3,4-Trifluoroanilino)propanolHCID 11401466—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDimethylformamideHCID 6228—
ProductDiethyl [2,3,4-trifluoro[(1S)-2-hydroxy-1-methylethyl]anilino]methylenemalonateHCID 1148565290.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

At room temperature, potassium hydroxide (330 mg) and tetrabutylammonium hydrogensulfate (82.7 mg) were dissolved in DMF (15 ml). After adding a solution (5 ml) of (2S)-2-(2,3,4-trifluoroanilino)propanol (1 g, 99.8% ee) and diethylethoxymethylenemalonate (2.09 g) in DMF, the resultant mixture was stirred for 1 hour. After adding water, the liquid reaction mixture was extracted with a solvent mixture of ethyl acetate and n-hexane (3:2). The organic layer was washed with water and dried over anhydrous magnesium sulfate. After evaporating the solvent, IPE was added to the obtained residue and the mixture was stirred at 0° C. for 1 hour. The crystals thus precipitated were collected by filtration and the moist product thus obtained was dried under reduced pressure. Thus, the title compound (1.65 g, 99. 8% ee) was obtained as colorless crystals. The 1H-NMR and IR spectral data of this product was identical with those of the compound obtained in Example 63.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087778B2
Source datasetuspto-grants-2006_08
ORD IDord-b70b5d96668a4a3a90823c7b62b9d362
Source noteuspto-grants-2006_08