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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

반응식

참여 물질

역할이름HCID투입량
반응물3,5,5-Trimethyl-1-hexanolHCID 18938—
반응물Sodium hydrideHCID 24758—
반응물2-(2H-Benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenolHCID 54751948—
용매1,4-DioxaneHCID 31275—
생성물2-(2H-Benzotriazol-2-yl)-4-methyl-6-(3,5,5-trimethylhexyloxymethyl)-phenolHCID 6729433149.1%

반응 조건

온도80 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883829B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-14eba43c76054600818d4866d6213859
출처 메모uspto-grants-2014_11