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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1951575생성일: 2026년 10월 27일

Pyridine → methyl 2-(N-benzyl-4-nitrobenzamido)-2-phenylacetate

https://huagongshe.com/reaction/1951575

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물4-Nitrobenzoyl chlorideHCID 8502—
반응물Methyl 2-(benzylamino)-2-phenylacetateHCID 3699844—
용매DichloromethaneHCID 6344—
생성물methyl 2-(N-benzyl-4-nitrobenzamido)-2-phenylacetateHCID 5746536896.4%

반응 단계

to a solution of methyl 2-(benzylamino)-2-phenylacetate (4.818 g, 18.9 mmol) and pyridine (15.3 ml, 189 mmol) in 75 mL dichloromethane cooled by an ice bath was added 4-nitrobenzoyl chloride (3.50 g, 18.9 mmol) all at once. The cold bath was removed and the reaction stirred to room temperature. The reaction was stirred at room temperature for four hours then concentrated under reduced pressure, taken up in 100 mL heptane and concentrated under reduced pressure. The concentrate was partitioned between 100 mL dichloromethane and 100 mL water. The organic separation was washed with 50 mL brine then stirred over magnesium sulfate, filtered and the filtrate concentrated under reduced pressure to afford a colorless oil. The product was purified by chromatography on silica, eluting with 10-30% ethyl acetate in hexane to afford a colorless foamy solid (7.37 g, 96%). ESI+ m/z=405.1 [MH]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08404722B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-b6a573e29af74cc0b7b8e84e531529b8
출처 메모uspto-grants-2013_03