HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892620Generated: October 26, 2026
Tetrahydrofuran → 3-(4-Ethoxycarbonyloxycinnamoyl)amino-epsilon-caprolactam
https://huagongshe.com/reaction/892620
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 3-(3-Hydroxy-4-methoxyphenyl)prop-2-enoic acid | HCID 92126 | — |
| Reactant | 4-Aminoazepan-2-one | HCID 21584138 | — |
| Product | 3-(4-Ethoxycarbonyloxycinnamoyl)amino-epsilon-caprolactam | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05118806 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-2f7299906dbe4a1e92167c16c3c5d7ce |
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| Source note | uspto-grants-1992_06 |
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