HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926822Generated: October 28, 2026
Triethylamine → 2-[2-(Benzyloxy)ethoxy]ethyl acrylate
https://huagongshe.com/reaction/926822
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | 2-[2-(Benzyloxy)ethoxy]ethan-1-ol | HCID 229722 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[2-(Benzyloxy)ethoxy]ethyl acrylate | HCID 66701901 | 84% |
Reaction Steps
To a 1 L three-neck round bottom flask equipped with mechanical stirrer were charged diethylene glycol monobenzyl ether (98.0 g, 0.5 mol), anhydrous triethylamine (120 mL, 0.85 mol), and anhydrous THF (300 mL). The solution was cooled in an ice/salt bath under dry air blanket for 15 minutes. Acryloyl chloride (55 mL, 0.68 mol) was added into the vigorously stirred cold solution through an addition funnel over 90 minutes and the addition rate was adjusted to keep the temperature of the reaction mixture below 10° C. After the addition, the reaction mixture was stirred in the ice/salt bath for additional two hours followed by quenching with the addition of 2M HCl (400 mL). The mixture was extracted with ethyl acetate (300 mL×3) and the combined organic layer was washed with DI water (200 mL×3), aqueous sodium bicarbonate (200 mL×2), and dried over MgSO4. Filtration and removal of solvents under reduced pressure gave the crude product as light brown oil which was purified on silica gel using Hexanes/Ethyl acetate (4/1, v/v) as eluent to give the final product as a colorless oil (105.0 g, 0.42 mol, yield: 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09289531B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-ca149ce7404d4030a736631683f787fd |
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| Source note | uspto-grants-2016_03 |
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