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HRID 8772생성일: 2026년 10월 23일

Triacetoxyperiodinane → tert-Butyl 4-(4-phenyl-1,3-dioxobut-1-yl)-4-(2-(tert-butyldimethylsilyloxy)eth-1-yl)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/8772

반응식

참여 물질

역할이름HCID투입량
반응물TriacetoxyperiodinaneHCID 159087—
반응물tert-Butyl 4-(4-phenyl-3-hydroxy-1-oxobut-1-yl)-4-(2-(tert-butyldimethylsilyloxy)eth-1-yl)piperidine-1-carboxylateHCID 21983965—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물tert-Butyl 4-(4-phenyl-1,3-dioxobut-1-yl)-4-(2-(tert-butyldimethylsilyloxy)eth-1-yl)piperidine-1-carboxylateHCID 2198397869.5%

반응 단계

To a solution of tert-butyl 4-(4-phenyl-3-hydroxy-1-oxobut-1-yl)-4-(2-(tert-butyldimethylsilyloxy)eth-1-yl)piperidine-1-carboxylate (494 mg, 0.98 mmol) from Step F in methylene chloride (10 mL) at room temperature was added Dess-Martin reagent (621 mg, 1.5 mmol). After 3 h, the reaction was diluted with ether and quenched with 1N sodium hydroxide. After stirring for 30 min, the mixture was diluted with water and extracted twice with ether. The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated. The residue was purified by flash chromatography (10% ethyl acetate in hexanes) to afford the title product (343 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091211B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-0ad6df59fec94b07b829b6f097e8956d
출처 메모uspto-grants-2006_08