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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 597649생성일: 2026년 10월 26일

Diethyl Ether → Cyclohexylsulfamate

https://huagongshe.com/reaction/597649

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물IsopropylamineHCID 6363—
반응물CyclamateHCID 7533—
반응물1-[p-(2-Acetylamino-2-carbomethoxyvinyl)-phenoxy]-2,3-epoxy-propaneHCID 54135887—
용매AcetoneHCID 180—
용매TetrahydrofuranHCID 8028—
생성물CyclohexylsulfamateHCID 3372845—
생성물1-[p-(2-Acetylamino-2-carbomethoxy-vinyl)-phenoxy]-2-hydroxy-3-isoproylamino-propaneHCID 53843743—

반응 단계

15.6 g (0.05 mol) of 1-[p-(2-acetylamino-2-carbomethoxyvinyl)-phenoxy]-2,3-epoxy-propane are dissolved in 50 ml of absolute tetrahydrofurane, 4.25 ml (0.05 mol) of isopropylamine are added and thereafter the mixture is heated for 18 hours to the boil under a reflux condenser. It is then evaporated in vacuo and the resulting crude base is dissolved in ethyl acetate. The solution is extracted three times with 20 ml of 1 N hydrochloric acid at a time. The hydrochloric acid extracts are brought to pH 8 with sodium carbonate solution and the crude base which hereupon has separated out is extracted with ethyl acetate. The extract is washed with water, dried over sodium sulphate and evaporated in vacuo. 17 g of crude base are obtained as a brownish oil. This is dissolved in 20 ml of acetone and mixed with a solution of 9 g of N-cyclo-hexylsulphamic acid in 70 ml of acetone. After addition of ether, the N-cyclohexylsulphamate of 1-[p-(2-acetylamino-2-carbomethoxy-vinyl)-phenoxy]-2-hydroxy-3-isoproylamino-propane, melting point 121°-125°C, is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04014920
출처 데이터셋uspto-grants-1977_03
ORD IDord-57711c621d6f41989b2a5d1e03163bce
출처 메모uspto-grants-1977_03