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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

反応式

関与物質

役割名称HCID仕込み量
反応物3,5,5-Trimethyl-1-hexanolHCID 18938—
反応物Sodium hydrideHCID 24758—
反応物2-(2H-Benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenolHCID 54751948—
溶媒1,4-DioxaneHCID 31275—
生成物2-(2H-Benzotriazol-2-yl)-4-methyl-6-(3,5,5-trimethylhexyloxymethyl)-phenolHCID 6729433149.1%

反応条件

温度80 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883829B2
出典データセットuspto-grants-2014_11
ORD IDord-14eba43c76054600818d4866d6213859
出典メモuspto-grants-2014_11