HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 886674Generated: October 27, 2026
Triethylamine → 2-(2-(2-Methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethyl methacrylate
https://huagongshe.com/reaction/886674
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | 2-(2-(2-Methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethanol | HCID 58105967 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-(2-Methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethyl methacrylate | HCID 57828741 | 97% |
Reaction Steps
A 2 liter 3-neck flask fitted with a thermometer, a cooling tube and a stirrer was charged with 165 g (584 mmol) of 2-(2-(2-methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethanol, 2,000 ml of THF, 105 ml (754 mmol) of triethylamine and 0.165 g (1,000 ppm) of p-methoxyphenol, and the mixture was stirred to form a solution. Following dissolution, the solution was cooled in an ice bath and 62.7 ml (648 mmol) of methacryloyl chloride was added gradually to the solution. The reaction mixture was then returned to room temperature, and stirred for 3 hours. Following completion of the reaction, 1,000 ml of diethyl ether was added, and the filtrate was washed 5 times with 200 ml samples of distilled water. The washed extract was then concentrated, yielding 198 g (yield: 97%, GC purity: 99%) of the targeted colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247160B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-f0f95afe8bbd4af1abe71613e713a4bf |
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| Source note | uspto-grants-2012_08 |
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