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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308030Generated: October 26, 2026

Triethylamine → 2-(2-Trifluoromethyl-2-propenoyloxy)-2-methyladamantane

https://huagongshe.com/reaction/2308030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Methyl-2-adamantanolHCID 136545—
Reactant2-(Trifluoromethyl)prop-2-enoyl chlorideHCID 10149016—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Trifluoromethyl-2-propenoyloxy)-2-methyladamantaneHCID 1130069270.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 500 ml flask was flushed with nitrogen to displace the air with nitrogen, and was charged with 83.1 g (0.50 mol) of 2-methyl-2-adamantanol, 101.2 g (1.0 mol) of triethylamine and 200 g of tetrahydrofuran. Then 118.9 g (0.75 mol) of α-trifluoromethylacryloyl chloride was dropwise added to the content in the flask over a period of about 1 hour, while the content was maintained at a reaction temperature of about 0° C. Then the content was stirred for 10 hours at room temperature. After completion of the reaction, the reaction mixture was washed with water and then with an aqueous saturated sodium chloride solution. The thus-obtained organic phase was subjected to column chromatography, and further, analyzed by NMR and mass spectrometry. Thus, 101.2 g (yield: 70.3%) of the object 2-methyl-2-adamantyl α-trifluoromethylacrylate was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833462B2
Source datasetuspto-grants-2004_12
ORD IDord-037f258cd14b4049990a9998f3b38c3f
Source noteuspto-grants-2004_12