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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 334834생성일: 2026년 10월 25일

2-Ethylhexanoic Acid → 2-Ethyl-hexanoic acid 3-(2H-benzotriazol-2-yl)-2-hydroxy-5-methyl-benzyl ester

https://huagongshe.com/reaction/334834

반응식

참여 물질

역할이름HCID투입량
반응물2-Ethylhexanoic AcidHCID 8697—
반응물Sodium CarbonateHCID 10340—
반응물2-(2H-Benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenolHCID 54751948—
용매TetrahydrofuranHCID 8028—
생성물2-Ethyl-hexanoic acid 3-(2H-benzotriazol-2-yl)-2-hydroxy-5-methyl-benzyl esterHCID 6729622389%

반응 조건

온도70 °C

반응 단계

2-(2H-Benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenol (10.0 g, 33 mmol) is suspended in a mixture of 2-ethylhexanoic acid (11.9 g, 82 mmol) and tetrahydrofuran (75 g) and stirred at 70° C. for 30 minutes. Sodium carbonate (10.5 g, 99 mmol) is added. The slightly yellow reaction mixture is stirred at 60° C. for 15 minutes and evaporated to dryness. The residue is dissolved in ethyl acetate and extracted with an aqueous potassium carbonate solution (10%) and brine. 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 11.2 g of 2-Ethyl-hexanoic acid 3-(2H-benzotriazol-2-yl)-2-hydroxy-5-methyl-benzyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883829B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-6cd398ffc4d44d75bea72023ea05bf74
출처 메모uspto-grants-2014_11