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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922454Generated: November 2, 2026

Tetrahydrofuran → 1-[4-Methoxy-3-(4-methoxybutyl)phenyl]ethanone

https://huagongshe.com/reaction/922454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantLithium ChlorideHCID 433294—
ReactantPotassium FluorideHCID 522689—
Reactant4-Bromo-1-methoxy-2-(4-methoxybutyl)benzeneHCID 21458627—
CatalystHCID 178418397HCID 178418397—
Product1-[4-Methoxy-3-(4-methoxybutyl)phenyl]ethanoneHCID 86707866—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-bromo-1-methoxy-2-(4-methoxybutyl)benzene (523 mg) in tetrahydrofuran (10 mL) were added lithium chloride (326 mg), tetrakis(triphenylphosphine)palladium (0) (381 mg) and tri-n-butyltin-1-ethoxyvinyl 91.11 mL), and the mixture was heated to stir at 80° C. for 20 hours. The reaction solution was cooled to room temperature, and then thereto was added aqueous potassium fluoride solution, and the mixture was stirred for 30 minutes. The mixture was extracted with diethyl ether, and then thereto was added 10% hydrochloric acid, and the mixture was stirred for 1 hour. The organic layer was separated, dried over magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1→1/1) to give 1-[4-methoxy-3-(4-methoxybutyl)phenyl]ethanone [REx(24-1)] (195 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278944B2
Source datasetuspto-grants-2016_03
ORD IDord-ec3db68129f646a68435292c7338880d
Source noteuspto-grants-2016_03