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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031889Generated: October 26, 2026

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

https://huagongshe.com/reaction/1031889

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04956360
Source datasetuspto-grants-1990_09
ORD IDord-3baf6b5e7e3c4515a9d7fe92b0380ee1
Source noteuspto-grants-1990_09