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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 895791생성일: 2026년 10월 24일

Sulfuric Acid → 1-Benzyl-4-phenylpiperidine-4-carboxamide

https://huagongshe.com/ko/reaction/895791

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Sodium HydroxideHCID 14798—
반응물1-Benzyl-4-cyano-4-phenylpiperidineHCID 191408—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물1-Benzyl-4-phenylpiperidine-4-carboxamideHCID 9642395%

반응 조건

온도60 °C

반응 단계

A mixture of 3 kg of commercial 1-benzyl-4-cyano-4-phenylpiperidine, 6 l of water, 8.98 l of toluene and 1.35 kg of an aqueous 35% sodium hydroxide solution is heated under nitrogen at 60° C. and the aqueous phase is separated out by settling at this temperature. The toluene phase is dried by azeotropic distillation and the solution thus obtained containing the 1-benzyl-4-cyano-4-phenylpiperidine base is added to a mixture of 2.83 kg of 95% sulfuric acid, 1.73 kg of glacial acetic acid and 3 l of toluene. The mixture thus obtained is heated for 6 hours, the heating is then stopped, the mixture is cooled to 60° C. and 3 l of water are added at this temperature. The mixture is allowed to cool to room temperature (about 20° C.) and is then poured into 8.65 l of 30% sodium hydroxide and 6.75 l of water. The temperature rises gradually to 75° C. The phases are separated by settling while hot and the organic phase is washed with water and dried azeotropically. The toluene solution is concentrated to half its volume and then cooled gradually to 60° C. and the crystallization is initiated. The crystallization is completed by cooling to 0° C. over 2 hours. The precipitate thus obtained is filtered off, washed and dried under vacuum at 60° C. 2.68 kg of 1-benzyl-4-phenyl-4-piperidinecarboxamide are thus obtained;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06916929B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-caf87a1502044bfe95fd5f63f7299f11
출처 메모uspto-grants-2005_07