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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1492996생성일: 2026년 10월 25일

Piperidine → 5-[2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-vinyl]-2,4-dihydro-[1,2,4]triazole-3-thione

https://huagongshe.com/reaction/1492996

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물3,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 73219—
반응물2-(5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)acetic acidHCID 178525260—
용매Pyridine tolueneHCID 22007288—
생성물5-[2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-vinyl]-2,4-dihydro-[1,2,4]triazole-3-thioneHCID 17844082833%

반응 단계

A solution of 2-(5-thioxo-4, 5-dihydro-1H-1,2,4-triazol-3-yl)acetic acid (prepared by the method described in Aust. J. Chem., 1979, 32, 161-5, Nowel W. Jacobsen, Bruce L. McCarthy, Stephanie Smith) (3.3 g, 0.021 mole) and 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzaldehyde (4.9 g, 0.021 mole) in a 2:1 mixture of toluene/pyridine (300 ml) is treated with piperidine (0.021 mole). The resulting mixture is stirred at reflux for 48 hours. The mixture is concentrated in vacuo and the residue dissolved in ether, the product is extracted from the organic phase with aqueous 1M NaOH. The combined aqueous layers are made acidic by treatment with aqueous 2M HCl, and the product extracted with a 1:1 mixture of ethyl acetate/ether. The organic layer is washed with saturated aqueous NaCl and dried over MgSO4. Filtration and concentration gives a solid which is triturated in hot isopropyl ether and filtered to provide 2.3 g (6.9 g theor., 33%) of desired (E)-2,4-dihydro-5-[2-[4-hydroxy-3,5-bis(1,1-dimethylethyl)phenyl]ethenyl]-3H-1,2,4-triazole-3-thione, mp 243° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05376670
출처 데이터셋uspto-grants-1994_12
ORD IDord-402093f87c3b4d58803c6ae32c442f15
출처 메모uspto-grants-1994_12