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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | 3,5-Di-tert-butyl-4-hydroxybenzaldehyde | HCID 73219 | — |
| 반응물 | 2-(5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)acetic acid | HCID 178525260 | — |
| 용매 | Pyridine toluene | HCID 22007288 | — |
| 생성물 | 5-[2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-vinyl]-2,4-dihydro-[1,2,4]triazole-3-thione | HCID 178440828 | 33% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05376670 |
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| 출처 데이터셋 | uspto-grants-1994_12 |
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| ORD ID | ord-402093f87c3b4d58803c6ae32c442f15 |
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| 출처 메모 | uspto-grants-1994_12 |
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