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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1165094생성일: 2026년 10월 27일

Water → 2,6,Di-tert-butyl-4-(3,7,11,15,tetramethyl-2-hexadecenyl)-phenol

https://huagongshe.com/reaction/1165094

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Boron trifluoride etherateHCID 8000—
반응물2,6-Di-tert-butylphenolHCID 31405—
반응물3,7,11,15-Tetramethylhexadec-2-en-1-olHCID 145386—
용매1,4-DioxaneHCID 31275—
생성물2,6,Di-tert-butyl-4-(3,7,11,15,tetramethyl-2-hexadecenyl)-phenolHCID 543969159.1%

반응 단계

A solution of 3,7,11,15-tetramethyl-2-hexadecen-1-ol (2.97 g;10.0 mmole) in dioxane (8 ml) was dropwise added to a solution of 2,6-di-tert-butyl phenol (4.13 g;200 mmole) and boron trifluoride ethyl etherate (0.86 g;6.0 mmole) in dioxane (20 ml) at 40° C. over one hour. After stirring the resultant solution at that temperature for 2.5 hours, the reaction solution was poured into water (30 ml) and was then extracted once with ethyl acetate (20 ml). The extract was successively washed with 30 ml of 5% (w/v) aqueous sodium hydroxide solution containing 3% (w/v) sodium hydrosulfite (once), 30 ml of water (twice) and then 30 ml of saturated aqueous sodium chloride (once) and was dried over anhydrous magnesium sulfate. Then, the solvent and the unreacted 2,6-di-tert-butyl-phenol were distilled off and the resultant residue was subjected to silica gel column chromatography to obtain 440 mg (0.91 mmole) of 2,6,di-tert-butyl-4-(3,7,11,15,tetramethyl-2 -hexadecenyl)-phenol from the fractions eluted through the column with hexane-ethyl acetate (50:1). Yield=9.1%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04906669
출처 데이터셋uspto-grants-1990_03
ORD IDord-dc848e1dbc56433eb75f9df13c754907
출처 메모uspto-grants-1990_03