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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48474생성일: 2026년 10월 24일

Triacetoxyperiodinane → Benzyl 3-formylpiperidine-1-carboxylate

https://huagongshe.com/ko/reaction/48474

반응식

참여 물질

역할이름HCID투입량
반응물TriacetoxyperiodinaneHCID 159087—
반응물benzyl (3R)-3-(hydroxymethyl)piperidine-1-carboxylateHCID 6932120—
용매DichloromethaneHCID 6344—
생성물Benzyl 3-formylpiperidine-1-carboxylateHCID 9899653—

반응 단계

To a stirring, 0° C. solution of 0.303 g (1.20 mmol) of 3-hydroxymethyl-piperidine-1-carboxylic acid benzyl ester (8) in CH2Cl2 (4.0 mL) was added 0.630 g (1.44 mmol) of Dess-Martin periodinane, and the solution was stirred under N2. When the reaction was complete by TLC (about 30 min.), the reaction was concentrated, and then Et2O was added. After standing for about 15 min., the reaction was filtered through Celite wet with Et2O, rinsed with Et2O, and concentrated. The crude reaction was purified by column chromatography (florisil®, 100-200 mesh, 2:1 Hexane: EtOAc) to achieve pure 9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703508B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-b2a037f8cccc4e88ae1cfed235e1c2c0
출처 메모uspto-grants-2004_03