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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700885Generated: November 1, 2026

2,6-Di-tert-butyl-4-methylphenol → 3-[4-[2-(N-Dodecyl-N-methylamino)ethoxy]-2-vinylphenyl]propanoic acid, methyl ester

https://huagongshe.com/reaction/1700885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
ReactantLithium ChlorideHCID 433294—
ReactantTri(butyl)vinyltinHCID 53438229—
Reactant3-[4-[2-(N-Dodecyl-N-methylamino)ethoxy]-2-[trifluoromethanesulfonyloxy]phenyl]propanoic Acid, Methyl EsterHCID 86757119—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product3-[4-[2-(N-Dodecyl-N-methylamino)ethoxy]-2-vinylphenyl]propanoic acid, methyl esterHCID 8675711882%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-[4-[2-(N-dodecyl-N-methylamino)ethoxy]-2-[trifluoromethanesulfonyloxy]-phenyl]propanoic acid, methyl ester (250 mg, 0.48 mmol) in 1,4-dioxane (2.5 ml) were added tributylvinyltin (1.2 ml, 4.0 mmol), lithium chloride (123 mg, 1.44 mmol), tetrakis(triphenylphosphine)-palladium(0) (10 mg) and 2,6-di-tert-butyl-4-methylphenol (10 mg). The resulting mixture was then stirred at 100° C. for 5 h. After cooling to r.t., the mixture was diluted with diethyl ether, washed with water, brine, dried over magnesium sulfate and concentrated in vacuo. The residue was chromatographed on silica gel (diethyl ether/acetone 100:0 to 80:20) to afford the title compound (170 mg, 80%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350892B1
Source datasetuspto-grants-2002_02
ORD IDord-e64aeeae9b4c41fdb65229373f0741ce
Source noteuspto-grants-2002_02