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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175765Generated: October 30, 2026

Ethyl Acetate → N-[4-(hydroxymethyl)phenyl]acrylamide

https://huagongshe.com/reaction/1175765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAcryloyl chlorideHCID 13140—
Reactant4-Aminobenzyl alcoholHCID 69331—
ReactantDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-(hydroxymethyl)phenyl]acrylamideHCID 1366154198.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

p-Aminobenzyl alcohol (12.31 g, 100 mmol) was dissolved in a mixture of dichloromethane (200 mL) and tetrahydrofuran (20 mL) containing N,N-diisopropylethylamine (35 mL, 200 mmol). The resulting homogeneous solution was then cooled to 0° C. and acryloyl chloride (8.2 mL, 100 mmol) was added drop-wise over a 30-minute period while keeping the internal temperature of the reaction mixture below 20° C. The reaction mixture was stirred at 0° C. for about 60 minutes. The reaction mixture was poured into ice-cold 1M hydrochloric acid (0.6 L) and the organic layer was separated and evaporated to dryness to give a crude material (5 g) consisting primarily of the bis-acylated side product. The acidic aqueous layer was then extracted with ethyl acetate (2×200 mL) and the combined ethyl acetate layers were dried with sodium sulfate, filtered and concentrated under reduced pressure to provide a residue. Trituration of the residue with ethyl acetate yielded the title compound (10.5 g, 98.5% pure). An additional 2 g of the title compound were obtained by trituration of the crude material obtained from the dichloromethane layer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842704B2
Source datasetuspto-grants-2010_11
ORD IDord-2d15c4f0e10d4d4a84af7e6d47c2defa
Source noteuspto-grants-2010_11