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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant2-[2-(Benzyloxy)ethoxy]ethan-1-olHCID 229722—
SolventTetrahydrofuranHCID 8028—
Product2-[2-(Benzyloxy)ethoxy]ethyl acrylateHCID 6670190184%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09289531B2
Source datasetuspto-grants-2016_03
ORD IDord-ca149ce7404d4030a736631683f787fd
Source noteuspto-grants-2016_03