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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1463465생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1463465

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. m.p. 209°-210°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05300639
출처 데이터셋uspto-grants-1994_04
ORD IDord-7aa84c2951954b5ba91866704b3fc3c7
출처 메모uspto-grants-1994_04