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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | 1-Ethyl-4-trifluoromethylcyclohexanol | HCID 64756511 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Ethyl-4-(trifluoromethyl)cyclohexyl methacrylate | HCID 67969261 | 75.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08535871B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-d932d86fdda44311868fb1815d018b40 |
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| Source note | uspto-grants-2013_09 |
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