Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 334829생성일: 2026년 10월 24일
3,5,5-Trimethyl-1-hexanol → 2-(2H-Benzotriazol-2-yl)-4-methyl-6-(3,5,5-trimethylhexyloxymethyl)-phenol
https://huagongshe.com/ko/reaction/334829
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3,5,5-Trimethyl-1-hexanol | HCID 18938 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2-(2H-Benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenol | HCID 54751948 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 2-(2H-Benzotriazol-2-yl)-4-methyl-6-(3,5,5-trimethylhexyloxymethyl)-phenol | HCID 67294331 | 49.1% |
반응 단계
2-(2H-Benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenol (7.0 g, 25.6 mmol) is partly solved in dioxane (190 mL) at 80° C. 3,5,5-Trimethyl-hexan-1-ol (124.1 g, 731 mmol) and sodium hydride (1.7 g, 42 mmol, 60% in mineral oil) are added subsequently. The orange reaction mixture is stirred at 80° C. for one hour and evaporated to dryness. The residue is dissolved in ethyl acetate and extracted with water. The organic layer is dried over sodium sulphate, filtered and evaporated to dryness. The crude product is purified by column chromatography (ethyl acetate/heptane 1:12) to yield 4.8 g of 2-(2H-Benzotriazol-2-yl)-4-methyl-6-(3,5,5-trimethylhexyloxymethyl)-phenol.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08883829B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-14eba43c76054600818d4866d6213859 |
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| 출처 메모 | uspto-grants-2014_11 |
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