돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1743260생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1743260

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물15-Crown-5HCID 36336—
반응물tert-butyl (2R,3S)-6-oxo-2,3-diphenylmorpholine-4-carboxylateHCID 981230—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물2-Trimethylsilanylethyl 4-iodopiperidine-1-carboxylateHCID 22238408—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl (3r,5r,6s)-2-oxo-5,6-diphenyl-3-[1-(2-trimethylsilanyl-ethoxycarbonyl)piperidin-4-yl]morpholine-4-carboxylateHCID 90791180—

반응 조건

온도-78 °C

반응 단계

4 g of tert-butyl (5S,6R)-2-oxo-5,6-diphenylmorpholine-4-carboxylate were dissolved in 50 ml of THF. 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-iodopiperidine-1-carboxylate were added dropwise. The mixture was allowed to warm to 0° C. over the course of 6 h, and then the reaction was stopped by adding 200 ml of saturated ammonium chloride solution. The aqueous phase was extracted 3 times with 150 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-3e41b89821224680bb8e0715a9e0af01
출처 메모uspto-grants-2006_03