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HRID 1165094作成日:2026年10月27日

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

https://huagongshe.com/reaction/1165094

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Boron trifluoride etherateHCID 8000—
反応物2,6-Di-tert-butylphenolHCID 31405—
反応物3,7,11,15-Tetramethylhexadec-2-en-1-olHCID 145386—
溶媒1,4-DioxaneHCID 31275—
生成物2,6,Di-tert-butyl-4-(3,7,11,15,tetramethyl-2-hexadecenyl)-phenolHCID 543969159.1%

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04906669
出典データセットuspto-grants-1990_03
ORD IDord-dc848e1dbc56433eb75f9df13c754907
出典メモuspto-grants-1990_03