돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 903453생성일: 2026년 10월 25일

Tetrahydrofuran → Ethyl gamma-cyano-gamma-[3-(trifluoromethyl)phenyl]-4-morpholinebutanoate

https://huagongshe.com/reaction/903453

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Ethyl AcrylateHCID 8821—
반응물2-Morpholino-2-[3-(trifluoromethyl)phenyl]acetonitrileHCID 3694192—
촉매Potassium HydroxideHCID 14797—
용매EthanolHCID 702—
생성물Ethyl gamma-cyano-gamma-[3-(trifluoromethyl)phenyl]-4-morpholinebutanoateHCID 12449509—

반응 단계

To a solution of 5.0 g. of α-[3-(trifluoromethyl)phenyl]-4-morpholineacetonitrile in 200 ml. of tetrahydrofuran stirred at room temperature is added 30 drops of 30% potassium hydroxide in ethanol. To the mixture is added 10 ml. of ethyl acrylate. After one hour an additional 30 drops of 30% potassium hydroxide in ethanol and 10 ml. of ethyl acrylate is added. The mixture is stirred for 2 hours and the solvent removed under vacuum. Toluene is added several times and the solvent removed. The residue is stirred with ether, filtered and the solvent evaporated to give ethyl γ-cyano-γ-[3-(trifluoromethyl)phenyl]-4-morpholinebutanoate (5.6 g.) as an oil. The oil is heated with 70% glacial acetic acid for 2 hours and the solvent removed. The residue is dissolved in dichloromethane and washed with water. The organic layer is dried (Na2SO4) and the solvent removed to give an oil. A mixture of the oil and 300 ml. of 6 N hydrochloric acid is refluxed for 5 hours, cooled and extracted with dichloromethane. The organic layer is extracted with sodium bicarbonate. The aqueous layer is acidified with concentrated hydrochloric acid and extracted with dichloromethane. The extract is dried (Na 2 SO4) and the solvent removed. The residue is crystallized from hexane to give 3-[3-trifluoromethylbenzoyl]propionic acid as crystals, mp. 80°-82° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04226775
출처 데이터셋uspto-grants-1980_10
ORD IDord-61b59cba0d30453cb1025ff577c22699
출처 메모uspto-grants-1980_10