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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2036098생성일: 2026년 10월 26일

Salicylamide → 1'-benzylspiro[1,3-benzoxazine-2,4'-piperidin]-4(3H)-one

https://huagongshe.com/reaction/2036098

반응식

참여 물질

역할이름HCID투입량
반응물SalicylamideHCID 5147—
반응물1-Benzyl-4-piperidoneHCID 19220—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
용매TolueneHCID 1140—
생성물1'-benzylspiro[1,3-benzoxazine-2,4'-piperidin]-4(3H)-oneHCID 379871—

반응 단계

Salicylamide (7.24 g), 1-benzylpiperidin-4-one (10.0 g) and p-toluenesulfonic acid hydrate (500 mg) were suspended in toluene (200 mL), and the suspension was stirred under reflux overnight while removing the water in the reaction system using a Dean-Stark tube. The mixture was cooled to room temperature, and the resulting precipitate was collected by filtration and washed with water, ethanol and diethyl ether to give 1′-benzylspiro[1,3-benzoxazine-2,4′-piperidin]-4(3H)-one as a crude product (9.7 g). The obtained crude 1′-benzylspiro[1,3-benzoxazine-2,4′-piperidin]-4(3H)-one (5.0 g) and 10% palladium-carbon (1.0 g) were suspended in ethanol (50 mL), and the suspension was stirred at 50° C. for 5 hr under a hydrogen atmosphere. The catalyst was removed by filtration through celite and the solvent was evaporated under reduced pressure. The resulting precipitate was collected by filtration, and washed with ethanol and diethyl ether to give the object product (2.7 g, 77%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08575167B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-afa3ae8ba5054595999672db83fd1ed5
출처 메모uspto-grants-2013_11