Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484935생성일: 2026년 10월 25일
Cyanuric chloride → 2-Chloro-4,6-bis-(2,2,6,6-tetramethyl-4-piperidyl-butylamino)-1,3,5-triazine
https://huagongshe.com/reaction/484935
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyanuric chloride | HCID 7954 | — |
| 반응물 | n-Butyl-2,2,6,6-tetramethyl-4-piperidinamine | HCID 118285 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 2-Chloro-4,6-bis-(2,2,6,6-tetramethyl-4-piperidyl-butylamino)-1,3,5-triazine | HCID 11114220 | — |
반응 단계
To a solution of 18.4 g of cyanuric chloride in 200 ml of dioxane was added dropwise, with stirring, a solution of 43.6 g of 4-butylamino-2,2,6,6-tetramethylpiperidine in 100 ml of dioxane at 20°-25° C. The mixture was stirred at the same temperature for 2 hours, after which it was stirred at 60°-70° C. for 2 hours. At the end of this time, the dioxane was distilled off and the residue was poured into a 10% aqueous solution of potassium carbonate and extracted with ethyl acetate. The extract was dried over anhydrous potassium carbonate, and then the ethyl acetate was distilled off. The resulting oil was purified by column chromatography through silica gel, eluted with a 20:1:1 by volume mixture of ethyl acetate, ethanol and triethylamine, to give the title compound in the form of crystals melting at 40°-42° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04533688 |
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| 출처 데이터셋 | uspto-grants-1985_08 |
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| ORD ID | ord-9da1fe9f6da34451a8adbe6533a12bd3 |
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| 출처 메모 | uspto-grants-1985_08 |
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