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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463465Generated: October 26, 2026

Tetrahydrofuran → 3-(4-Ethoxycarbonyloxycinnamoyl)amino-epsilon-caprolactam

https://huagongshe.com/reaction/1463465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant3-(3-Hydroxy-4-methoxyphenyl)prop-2-enoic acidHCID 92126—
Reactant4-Aminoazepan-2-oneHCID 21584138—
Product3-(4-Ethoxycarbonyloxycinnamoyl)amino-epsilon-caprolactamHCID 53856471—

Reaction Steps

Ethyl chloroformate (22.2 ml) was added dropwise to a mixture of 3-hydroxy-4-methoxycinnamic acid (22.5 g), triethylamine (32.3 ml) and THF (400 ml) under ice-cooling and stirring, followed by stirring for 15 mins. Subsequently, to the mixture was added dropwise a solution of 3-amino-ε-caprolactam (14.9 g) in THF (200 ml), and then the whole was stirred for 1 hr. at room temperature. After completing the dropping, the reaction mixture was concentrated under reduced pressure, and the residue was dissolved in chloroform. This solution was washed with water, dried and distilled under reduced pressure to remove the solvent. The residue was washed with ethyl acetate, dried under reduced pressure to give the title compound (28 g). This compound was used in the following reaction without purification. m.p. 209°-210°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300639
Source datasetuspto-grants-1994_04
ORD IDord-7aa84c2951954b5ba91866704b3fc3c7
Source noteuspto-grants-1994_04