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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776002Generated: October 30, 2026

Triethylamine → HCID 86685814, compound

https://huagongshe.com/reaction/1776002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethacryloyl chlorideHCID 13528—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant3,3,3-Trifluoro-2-hydroxypropanoic acidHCID 244896—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86685814HCID 8668581435%

Reaction Steps

Under a nitrogen atmosphere, 50 mL of dehydrated THF, 5.56 g (55.0 mmol) of triethylamine and 305 mg (2.5 mmol) of dimethylaminopyridine were added to 7.20 g (50.0 mmol) of 3,3,3-trifluorolactic acid at a room temperature. Thereafter, 5.75 g (55.0 mmol) of methacrylic acid chloride was added dropwise over 10 min, and then the mixture was stirred for 2 hrs. After disappearance of the raw material was confirmed by TLC, an aqueous sodium bicarbonate solution was added to stop the reaction. Thereafter, ethyl acetate was added to the reaction liquid and extraction was carried out three times. The organic layer thus obtained was washed with water, saturated brine each once, and dried by adding anhydrous sodium sulfate. Thereafter, the solvent was distilled off under a reduced pressure, and the resulting product was purified by column chromatography to give 3.71 g of 3,3,3-trifluoro-2-(methacryloyloxy)propionic acid represented by the following formula in the form of pale yellow oil (yield: 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09261780B2
Source datasetuspto-grants-2016_02
ORD IDord-403ae7d9acdf4913872c6a09931e24bd
Source noteuspto-grants-2016_02