돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 255889생성일: 2026년 10월 25일

Tetrahydrofuran → 4-(4-Morpholino-3-nitrophenyl)-4-(cyano)-4-(morpholino)-3-methylbutyronitrile

https://huagongshe.com/reaction/255889

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Potassium HydroxideHCID 14797—
반응물CrotononitrileHCID 637921—
반응물alpha-Morpholino-alpha(4-morpholino-3-nitrophenyl)-acetonitrileHCID 21855724—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물4-(4-Morpholino-3-nitrophenyl)-4-(cyano)-4-(morpholino)-3-methylbutyronitrileHCID 20164991—

반응 단계

A solution of 8.0 parts of crotononitrile in 20 parts by volume of tetrahydrofuran is added to a stirred mixture of 16.5 parts of α-morpholino-α(4-morpholino-3-nitrophenyl)-acetonitrile in 150 parts by volume of tetrahydrofuran and 1.5 parts of potassium hydroxide in 5 parts by volume of methanol at room temperature under an atmosphere of nitrogen. The reaction mixture is stirred for a further 6 hours, diluted with 500 parts by volume of water and extracted with 4×250 parts by volume of ethyl acetate. The combined organic extracts are dried over magnesium sulphate and concentrated under vacuum. The resulting crude product is triturated with a mixture of 50 parts by volume of ethyl acetate and hexane. The solid product is collected, washed with ethyl acetate and dried at 80° under vacuum to give 4-(4-morpholino-3-nitrophenyl)-4-(cyano)-4-(morpholino)-3-methylbutyronitrile having melting point 175°-177° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04699908
출처 데이터셋uspto-grants-1987_10
ORD IDord-34f3dbb82e4147ccac19e4dc74d3b950
출처 메모uspto-grants-1987_10