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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1743248생성일: 2026년 10월 27일

Allyl bromide → Tert-butyl (3s,5s,6r)-3-allyl-2-oxo-5,6-diphenylmorpholine-4-carboxylate

https://huagongshe.com/reaction/1743248

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물Ammonium ChlorideHCID 25517—
반응물tert-butyl (2R,3S)-6-oxo-2,3-diphenylmorpholine-4-carboxylateHCID 981230—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl (3s,5s,6r)-3-allyl-2-oxo-5,6-diphenylmorpholine-4-carboxylateHCID 11058313—

반응 조건

온도-78 °C

반응 단계

10 g of tert-butyl (5S,6R)-2-oxo-5,6-diphenylmorpholine-4-carboxylate were dissolved in 200 ml of THF and cooled to −78° C. 63 ml of a 0.5 M solution of KHMDS in toluene were added dropwise and, after stirring for 10 min, 3.7 ml of allyl bromide were added dropwise. The mixture was allowed to warm from −78° C. to −20° C. over the course of 3 h, and the reaction was then stopped by adding 300 ml of a saturated ammonium chloride solution. 200 ml of ethyl acetate were added, and the phases were separated. The aqueous phase was extracted 3 times with 100 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 stirred with diisopropyl ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07008957B2
출처 데이터셋uspto-grants-2006_03
ORD IDord-9f364c30dc6f4b19af11cf7bacabaeaa
출처 메모uspto-grants-2006_03