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HRID 1657063作成日:2026年10月27日

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/1657063

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物3,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 73219—
反応物2-(5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)acetic acidHCID 178525260—
溶媒Pyridine tolueneHCID 22007288—
生成物5-[2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-vinyl]-2,4-dihydro-[1,2,4]triazole-3-thioneHCID 17844082833%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05256680
出典データセットuspto-grants-1993_10
ORD IDord-ebdc466cc8bf41e1a0395a91f2a12e6d
出典メモuspto-grants-1993_10