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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25682생성일: 2026년 10월 24일

Diphenylacetaldehyde → tert-butyl ((4R)-2-benzhydryl-4-phenyl-oxazolidin-3-yl)-acetate

https://huagongshe.com/ko/reaction/25682

반응식

참여 물질

역할이름HCID투입량
반응물DiphenylacetaldehydeHCID 13696—
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물tert-butyl (S)-(2-hydroxy-1-phenyl-ethylamino)-acetateHCID 59065869—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물tert-butyl ((4R)-2-benzhydryl-4-phenyl-oxazolidin-3-yl)-acetateHCID 69754033114.1%

반응 단계

To a solution of tert-butyl (S)-(2-hydroxy-1-phenyl-ethylamino)-acetate (2.5 g, 10 mmole, obtained from Reference Example 9) in anhydrous methylene chloride (35 ml) were added diphenylacetaldehyde (2.16 g, 11 mmole) and magnesium sulfate (1.2 g, 10 mmole) under nitrogen. The resulting mixture was stirred at room temperature under nitrogen for 15 h, and diluted with ether. The organic layer was washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to dryness in vacuo. The oily residue was solidified upon standing, and recrystallized from ether/hexanes to give tert-butyl ((4R)-2-benzhydryl-4-phenyl-oxazolidin-3-yl)-acetate as a white solid (4.9 g, 98%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858591B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-baf8df1b87c8452ebbf4cdc0f2992acd
출처 메모uspto-grants-2005_02