HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44126Generated: October 26, 2026
Triethylamine → 2-(2-(2-Methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethyl methacrylate
https://huagongshe.com/reaction/44126
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
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 were added to and dissolved in a 2 L three-necked flask equipped with a thermometer, a cooling pipe, and a stirrer. Following completion of the dissolution, 62.7 mL (648 mmol) of methacryloyl chloride was gradually added thereto while cooling in an ice bath. The temperature of the resultant was then elevated to room temperature, and the resultant was stirred for 3 hours. Following the completion of the reaction, 1,000 mL of diethyl ether was added thereto, followed by washing with 200 mL of distilled water 5 times. Thereafter, the extraction liquid was concentrated, thereby obtaining 198 g of an objective substance (namely, a compound 3 having the following structure) in the form of a colorless liquid (yield: 97%, GC purity: 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541157B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-ed19f7c11f3d4a8095282b42ad8ac6c4 |
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| Source note | uspto-grants-2013_09 |
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