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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1715251생성일: 2026년 10월 27일

Triethylamine → Tert-butyl [3-(4,4-dimethyl-1,3-oxazolidin-3-yl)-3-oxopropyl]carbamate

https://huagongshe.com/reaction/1715251

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4,4-Dimethyl oxazolidineHCID 62010—
반응물N-((1,1-dimethylethoxy)carbonyl)-beta-alanineHCID 76809—
반응물2-Chloro-1-methylpyridinium iodideHCID 167069—
용매DichloromethaneHCID 6344—
용매Cyclohexane ethylacetateHCID 21867204—
생성물Tert-butyl [3-(4,4-dimethyl-1,3-oxazolidin-3-yl)-3-oxopropyl]carbamateHCID 86621990139.5%

반응 단계

To a mixture of 4,4-dimethyloxazolidine (287 μl; 2 mmol; 1 eq) and boc-beta-alanine (416.3 mg; 2.2 mmol; 1.10 eq) in DCM (30 ml), are added triethylamine (832 μl; 6 mmol; 3 eq) and 2-chloro-1-methylpyridinium iodide (1533 mg; 6 mmol; 3 eq). The mixture is stirred for 2 days at RT. The reaction is followed by TLC cyclohexane/EtOAc 1:1). The reaction mixture is then washed twice with NH4Cl sat. solution and twice with NaHCO3 sat. solution. The organic layer is dried over Na2SO4, filtered and concentrated to give 760 mg of an orange oil, which is purified by flash chromatography (cyclohexane/EtOAc gradient, from 9/1 to 1/1 over 30 min). The title product is isolated as a white-off solid (420.5 mg; 77%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07799814B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-aebc291accbd4055ad19e939995446b1
출처 메모uspto-grants-2010_09