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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5290Generated: October 25, 2026

Hydrochloric Acid → 2-(3,4,5-Triacetoxybenzamido)ethyl methacrylate

https://huagongshe.com/reaction/5290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantAminoethyl methacrylate hydrochlorideHCID 75495—
Reactant3,4,5-Triacetoxybenzoyl chlorideHCID 155506—
SolventDichloromethaneHCID 6344—
Product2-(3,4,5-Triacetoxybenzamido)ethyl methacrylateHCID 19795468—

Reaction Steps

3,4,5-Triacetoxybenzoyl chloride (0.050 mol) was dissolved in 100 mL CH2Cl2 at 0° C. To this was added 2-aminoethyl methacrylate hydrochloride (8.28 g, 0.050 mol), followed by dropwise addition of triethylamine (14.63 mL, 0.105 mol). After 30 min, 100 mL 1N HCl was added with vigorous stirring. The organic layer was isolated, washed with saturated NaHCO3 and 50 mL 1N HCl, dried over MgSO4, and evaporated to give an oil, which crystallized rapidly after the addition of 50 mL diethyl ether. The product was isolated by filtration and vacuum dried. Yield, 17.97 g as a white solid, 88%. 1H NMR (300 MHz, CDCl3), δ1.92 (s, 3H), 2.26 (s, 6H), 2.27 (s, 3H), 3.68 (m, 2H), 4.30 (t, 2H), 5.58 (m, 1H), 6.11 (s, 1H), 6.66 (t, broad, 1H), 7.51 (s, 2H). Anal., calcd for C19H21N1O9C 56.02, H 5.20, N 3.44, found C 55.99, H 5.15, N 3.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244763
Source datasetuspto-grants-1993_09
ORD IDord-a06527d7605c46b0b8ec403e13acd486
Source noteuspto-grants-1993_09