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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1803977생성일: 2026년 10월 25일

N,N'-Dimethylethylenediamine → methyl (R)-2-methoxy-4-(4-methyl-2-oxooxazolidin-3-yl)benzoate

https://huagongshe.com/reaction/1803977

반응식

참여 물질

역할이름HCID투입량
반응물N,N'-DimethylethylenediamineHCID 8070—
반응물Potassium CarbonateHCID 11430—
반응물(R)-4-Methyloxazolidin-2-oneHCID 2734858—
반응물Methyl 4-bromo-2-methoxybenzoateHCID 15128242—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물methyl (R)-2-methoxy-4-(4-methyl-2-oxooxazolidin-3-yl)benzoateHCID 67380952—

반응 단계

To a mixture of methyl 4-bromo-2-methoxybenzoate (5.8 mL), (R)-4-methyloxazolidin-2-one (2 g) described in Preparation Example 25, potassium carbonate (2.8 g) and copper (I) iodide (760 mg) were added toluene (10 mL) and N,N′-dimethylethylenediamine (880 μL), and the mixture was refluxed for 8 hr. After cooling, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, and the solvent was evaporated. The residue was purified by column chromatography (hexane:ethyl acetate) to give methyl (R)-2-methoxy-4-(4-methyl-2-oxooxazolidin-3-yl)benzoate (2.1 g). Methyl (R)-2-methoxy-4-(4-methyl-2-oxooxazolidin-3-yl)benzoate (2.1 g) was dissolved in methanol (8 mL) and tetrahydrofuran (8 mL), 1N aqueous sodium hydroxide solution (16 mL) was added, and the mixture was stirred at room temperature for 3 hr. 1N hydrochloric acid (16 mL) was added, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, and the solvent was evaporated. The title compound (2.2 g) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354401B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-d41c5d71014b4838a42e2ed6dfd84f18
출처 메모uspto-grants-2013_01