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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1165094Erstellt: 26. Oktober 2026

Water → HCID 54396915, Verbindung

https://huagongshe.com/reaction/1165094

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktBoron trifluoride etherateHCID 8000—
Edukt2,6-Di-tert-butylphenolHCID 31405—
Edukt3,7,11,15-Tetramethylhexadec-2-en-1-olHCID 145386—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktHCID 54396915HCID 543969159,1%

Reaktionsschritte

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%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04906669
Quelldatensatzuspto-grants-1990_03
ORD IDord-dc848e1dbc56433eb75f9df13c754907
Quellennotizuspto-grants-1990_03