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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1743267생성일: 2026년 10월 27일

Ammonium Chloride → Tert-butyl (3s,5s,6r)-3-allyl-2-oxo-5,6-diphenyl-3-[1-(2-trimethylsilanyl-ethoxycarbonyl)piperidin-4-ylmethyl]morpholine-4-carboxylate

https://huagongshe.com/reaction/1743267

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물15-Crown-5HCID 36336—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물Tert-butyl (3s,5s,6r)-3-allyl-2-oxo-5,6-diphenylmorpholine-4-carboxylateHCID 11058313—
반응물2-Trimethylsilanylethyl 4-bromomethyl-piperidine-1-carboxylateHCID 22238394—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl (3s,5s,6r)-3-allyl-2-oxo-5,6-diphenyl-3-[1-(2-trimethylsilanyl-ethoxycarbonyl)piperidin-4-ylmethyl]morpholine-4-carboxylateHCID 91566876—

반응 조건

온도-78 °C

반응 단계

4.9 g of tert-butyl (3S,5S,6R)-3-allyl-2-oxo-5,6-diphenylmorpholine-4-carboxylate were dissolved in 100 ml of THF. 14.9 ml of 15-crown-5 were added, and the mixture was cooled to −78° C. Then 6.8 ml of a 2 M solution of NaHMDS in THF were added dropwise. The mixture was stirred for 10 min and then 8 g of 2-trimethylsilanylethyl 4-bromomethylpiperidine-1-carboxylate were added dropwise. The mixture was allowed to warm to 0° C. over the course of 6 h, and the reaction was then stopped by adding 500 ml of saturated ammonium chloride solution. The aqueous phase was extracted 3 times with 400 ml of ethyl acetate each time, and the combined organic phases were dried with MgSO4. The solvents were removed in vacuo, and the residue was chromatographed on silica gel.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07008957B2
출처 데이터셋uspto-grants-2006_03
ORD IDord-c763f98885134e59bb54f39f86b5311f
출처 메모uspto-grants-2006_03