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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165094Generated: October 25, 2026

Water → HCID 54396915, compound

https://huagongshe.com/reaction/1165094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBoron trifluoride etherateHCID 8000—
Reactant2,6-Di-tert-butylphenolHCID 31405—
Reactant3,7,11,15-Tetramethylhexadec-2-en-1-olHCID 145386—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 54396915HCID 543969159.1%

Reaction Steps

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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906669
Source datasetuspto-grants-1990_03
ORD IDord-dc848e1dbc56433eb75f9df13c754907
Source noteuspto-grants-1990_03