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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264785Generated: October 27, 2026

Diethyl Ether → t-Butyl 3-{6-hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoate

https://huagongshe.com/reaction/264785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactanttert-Butyl acrylateHCID 15458—
ReactantPotassium AcetateHCID 517044—
Reactant2-Bromo-6-hydroxymethyl-[8(4-methoxyphenyl)octyloxy]pyridineHCID 19692711—
CatalystTetrabutylammonium IodideHCID 67553—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Productt-Butyl 3-{6-hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoateHCID 54231524—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 2-bromo-6-hydroxymethyl-[8(4-methoxyphenyl)octyloxy]pyridine (5.00 g, 11.8 mmol) in DMF (22.8 ml) and water (1.2 ml) were added potassium acetate (3.00 g, 30.6 mmol), tetra-n-butylammonium iodide (4.36 g, 11.8 mmol), bis(triphenylphosphine)palladium dichloride (0.33 g, 0.47 mmol) and t-butyl acrylate (6.16 g, 48 mmol). The mixture was placed under nitrogen and stirred and heated at 120° C. for 45 min. The mixture was cooled and added to water (250 ml). The product was extracted into ethyl acetate (2×60 ml). The combined extracts were washed with water (100 ml), 5% sodium chloride solution (2×100 ml), then dried and evaporated. The product was obtained by flash column chromatography using silica and 10% ether in dichloromethane. Yield 4.29 g, 77%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646286
Source datasetuspto-grants-1997_07
ORD IDord-f063d2f24f07467ba7c8464fbfc5ad1d
Source noteuspto-grants-1997_07