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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 476344생성일: 2026년 10월 24일

Pyridine → N,N-bis(4-methoxyphenyl)-2-oxopropanamide

https://huagongshe.com/ko/reaction/476344

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Pyruvic AcidHCID 1060—
반응물4,4'-DimethoxydiphenylamineHCID 7571—
반응물Thionyl ChlorideHCID 24386—
용매TetrahydrofuranHCID 8028—
생성물N,N-bis(4-methoxyphenyl)-2-oxopropanamideHCID 5760812982.4%

반응 단계

Pyruvic acid (1.00 g, 11.34 mmol) was placed in a 250 mL three-necked round-bottomed flask fitted with a stirring bar, reflux condenser and a nitrogen inlet, and dissolved in 30 mL anhydrous THF at room temperature. Then, SOCl2 (2.03 g, 17.01 mmol) was added dropwise with stirring in 3 hours at room temperature. Bis(4-methoxyphenyl)amine (2.00 g, 8.72 mmol) was added under nitrogen protection. Pyridine (4.14 g, 52.3 mmol) were added to the mixture at 0° C. The reaction mixture was heated to reflux for 12 hours. The reaction was quenched by adding 30 mL of 2N HCl solution. The mixture was extracted with EtOAc (3×20 mL). The organic layers were separated, washed with brine (20 mL) and dried over anhydrous MgSO4. The solvent was removed under reduced pressure to give a yellow residue. The solvent was removed and residue was subjected to flash column chromatography (silica gel, EtOAc/hexanes=3/7 v/v) to give a white solid product, N,N-bis(4-methoxyphenyl)-2-oxopropanamide, 2.15 g, 82.4% yield. MS: m/z 322 [M+Na]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637706B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-f4f649e9303449fcbbd1e04727cd0899
출처 메모uspto-grants-2014_01