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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41846Generated: October 26, 2026

Triethylamine → 1-Ethyl-4-(trifluoromethyl)cyclohexyl methacrylate

https://huagongshe.com/reaction/41846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethacryloyl chlorideHCID 13528—
Reactant1-Ethyl-4-trifluoromethylcyclohexanolHCID 64756511—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetoneHCID 180—
Product1-Ethyl-4-(trifluoromethyl)cyclohexyl methacrylateHCID 6796926175.7%

Reaction Steps

A four-necked flask equipped with a stirrer, a thermometer, and a dropping funnel was charged with 7.9 g (0.04 mol) of 1-ethyl-4-trifluoromethylcyclohexanol, 0.2 g of 4-dimethylaminopyridine, 4.9 g of triethylamine, and 20 g of acetone. The mixture was stirred to obtain a solution. A solution prepared by dissolving 4.6 g (0.044 mol) of methacrylic acid chloride in 5 g of acetone was added to the solution at 4° C. over 30 minutes. The mixture was stirred at 4° C. for 3 hours to obtain a reaction mixture. The reaction mixture was washed with water to obtain 8.0 g of 1-ethyl-4-(trifluoromethyl)cyclohexyl methacrylate (hereinafter may be referred to as “compound (M-3)” ((M-3) in Table 1)). The yield of 1-ethyl-4-(trifluoromethyl)cyclohexyl methacrylate with respect to 1-ethyl-4-trifluoromethylcyclohexanol was 76%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08535871B2
Source datasetuspto-grants-2013_09
ORD IDord-d932d86fdda44311868fb1815d018b40
Source noteuspto-grants-2013_09