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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709717Generated: October 25, 2026

Pyridine → Capryloyloxyethyl acrylate

https://huagongshe.com/reaction/1709717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiethyl EtherHCID 3283—
ReactantAcryloyl chlorideHCID 13140—
ReactantPolyethylene glycol monocaprylateHCID 170609—
SolventBenzeneHCID 241—
ProductCapryloyloxyethyl acrylateHCID 54523676—

Reaction Steps

A solution of 2-hydroxyethyl caprylate (HEC) (1 mol; 188.3 g) in pyridine (1.25 mol; 98.9 g; 100.7 ml) was added under continuous stirring at 5°-10° C. into a solution of freshly distilled acryloyl chloride (1.12 mol; 101.4 g) in benzene (300 ml). The mixture was further stirred for 2 hours at the reaction temperature, extracted with 800 ml of 2% hydrochloric acid, the emulsion formed was broken by addition of ether and the aqueous layer was repeatedly extracted with ether until the reaction on capryloyloxyethyl acrylate was negative. The combined ether extracts were washed with water, solution of potassium hydrogencarbonate (KHCO3), and water and dried with magnesium sulfate (MgSO4). Ether was removed by distillation under normal pressure and the product was distilled after addition of octylpyrocatechol as an inhibitor. The overall yield of raw product was 74.9%. The obtained fractions contained 60 to 93% of capryloyloxyethyl acrylate. The product with purity 99.8% was obtained by redistillation; b.p. 111° C./66.7 Pa. Elemental analysis for C13H22O4 theory: 64.44% C, 9.15% H; found 64.23% C; 9.41% H. The infrared and 13C-NMR spectra proved the expected structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950733
Source datasetuspto-grants-1990_08
ORD IDord-1c5fac6161984213ab5abff5cfdeb26e
Source noteuspto-grants-1990_08