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HRID 334829作成日:2026年10月25日
3,5,5-Trimethyl-1-hexanol → 2-(2H-Benzotriazol-2-yl)-4-methyl-6-(3,5,5-trimethylhexyloxymethyl)-phenol
https://huagongshe.com/reaction/334829
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3,5,5-Trimethyl-1-hexanol | HCID 18938 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2-(2H-Benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenol | HCID 54751948 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 2-(2H-Benzotriazol-2-yl)-4-methyl-6-(3,5,5-trimethylhexyloxymethyl)-phenol | HCID 67294331 | 49.1% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08883829B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-14eba43c76054600818d4866d6213859 |
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| 出典メモ | uspto-grants-2014_11 |
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