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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46808생성일: 2026년 10월 24일

Benzaldehyde → Benzamide, 2-(hydroxyphenylmethyl)-N-methyl-

https://huagongshe.com/ko/reaction/46808

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물N-MethylbenzamideHCID 11954—
반응물Ammonium ChlorideHCID 25517—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Benzamide, 2-(hydroxyphenylmethyl)-N-methyl-HCID 12241019—

반응 조건

온도5 °C

반응 단계

To a flask equiped with a stirrer, dropping funnel, condenser and gas inlet tube maintained under a nitrogen atmosphere there is added at room temperature 67.5 g. (0.5 mole) N-methyl benzamide and 1200 ml. dry tetrahydrofuran. The reaction flask is immersed in an ice bath and cooled to an internal temperature of 5° C. Stirring is initiated and 688 ml. of 1.6 M. n-butyl lithium (1.1 mole) in hexane is added dropwise over about 1 hour maintaining temperature below 8° C. The resulting dilithio salt is stirred at 5° C. for an additional hour and then a solution of 58.5 g. (0.55 mole) of benzaldehyde in 500 ml. tetrahydrofuran is added dropwise in about 1 hour maintaining the temperature between -10° to +10° C. The resulting mixture is stirred at 5° C. for 1 hour longer and 300 ml. of saturated ammonium chloride is added maintaining the temperature at about 10° C. The layers are separated and the organic phase dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to give α-hydroxy-N-methyl-α-phenyl-o-toluamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04175191
출처 데이터셋uspto-grants-1979_11
ORD IDord-6721723cd52743ab8e7c7fc23665ee85
출처 메모uspto-grants-1979_11