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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1031889생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1031889

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물3-(3-Hydroxy-4-methoxyphenyl)prop-2-enoic acidHCID 92126—
반응물4-Aminoazepan-2-oneHCID 21584138—
생성물3-(4-Ethoxycarbonyloxycinnamoyl)amino-epsilon-caprolactamHCID 53856471—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04956360
출처 데이터셋uspto-grants-1990_09
ORD IDord-3baf6b5e7e3c4515a9d7fe92b0380ee1
출처 메모uspto-grants-1990_09