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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1260939생성일: 2026년 10월 24일

Dimethylformamide → (4R)-4-benzyl-3-[(2E)-3-(3,4-dichlorophenyl)prop-2-enoyl]-1,3-oxazolidin-2-one

https://huagongshe.com/ko/reaction/1260939

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물3,4-Dichlorocinnamic acidHCID 688027—
용매TetrahydrofuranHCID 8028—
생성물(4R)-4-benzyl-3-[(2E)-3-(3,4-dichlorophenyl)prop-2-enoyl]-1,3-oxazolidin-2-oneHCID 6887314549%

반응 단계

To a solution of (2E)-3-(3,4-dichlorophenyl)prop-2-enoic acid (5.0 g) and DMF (178 μL) in THF (115 mL) was added oxalyl chloride (3.98 mL) at room temperature, and the mixture was stirred for 45 min. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in THF (13.8 mL). The THF solution was added dropwise to a solution of (4R)-4-benzyl-1,3-oxazolidin-2-one (4.48 g), triethylamine (15.9 mL) and LiCl (4.87 g) in THF (115 mL) at 0° C., and the mixture was stirred overnight at room temperature. The reaction mixture was poured into water, and the resultant product was extracted with ethyl acetate. The organic layer was washed with water and brine and dried, and the solvent was evaporated under reduced pressure to give (4R)-4-benzyl-3-[(2E)-3-(3,4-dichlorophenyl)prop-2-enoyl]-1,3-oxazolidin-2-one (4.22 g, 49%) as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08470816B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-260d271a6c8d4170ae367f8900ecc734
출처 메모uspto-grants-2013_06