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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589095Generated: November 3, 2026

Hydrochloric Acid → HCID 13579306, compound

https://huagongshe.com/reaction/1589095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantm-TrifluoromethylphenylacetonitrileHCID 75360—
Reactant(L)-ethyl lactateHCID 92831—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 13579306HCID 1357930618.3%

Reaction Steps

A dry, 500-ml, three-neck, round-bottom flask equipped with a mechanical stirrer, addition funnel and a reflux condenser was charged with 100 ml of ethanol. To the stirred solvent were added 3.5 g of sodium. After all the metal had dissolved, a solution of 13.0 g of ethyl L-(+)-lactate and 18.5 g of m-trifluoromethylphenylacetonitrile in 30 ml of ethanol was added dropwise to the reaction mixture. The mixture became a deep red and after the addition was complete, the mixture was heated at reflux overnight (about 18 hours). The mixture was then cooled to room temperature and added to 300 ml of water and the resulting mixture was acidified (pH about 1) with 10% hydrochloric acid. The mixture was then extracted with ether (three times) and the organic extracts were washed (two times) with saturated aqueous sodium bicarbonate, dried over magnesium sulfate and concentrated in vacuo to yield a thick oil. This oil was taken up in a mixture of ether/petroleum ether and the desired compound crystallized as a yellow powder. Two crops of crystals were collected to afford a total of 4.7 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04568376
Source datasetuspto-grants-1986_02
ORD IDord-40b7fdf996404f1ca1a851682ee11487
Source noteuspto-grants-1986_02