Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356641Generated: October 26, 2026

Diethyl Ether → HCID 18938971, compound

https://huagongshe.com/reaction/356641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant5-Bromo-2-methoxybenzaldehydeHCID 90684—
ReactantPotassium FluorideHCID 522689—
ReactantStannane, tributyl(1-methylethenyl)-HCID 10871254—
SolventTolueneHCID 1140—
ProductHCID 18938971HCID 18938971—

Reaction Steps

Tri-n-butyl-isopropenyltin (12.1 g, 36.6 mmol) dissolved in toluene (10 ml) was added to a mixture of 5-bromo-o-anisaldehyde (6.00 g, 27.9 mmol), tetrakis (triphenylphosphine)palladium (1.21 g, 1.05 mmol), and 2,6-t-butyl4-methylphenol (10 mg) in toluene (50 ml) under nitrogen at room temperature. This mixture was heated at reflux for 7 hr. Ether and aq. KF solution (80 ml) were added to the reaction mixture, and the resulting solution was stirred for 3 hr. Insoluble materials were removed by filtration through Celite. The filtrate was extracted with ether, and the organic phase was washed with 1N-NaHSO4 aq. NaHCO3 and brine. The extracts were dried over Na2SO4, and concentrated by evaporation. The residual oil was purified by chromatography (SiO2, 140 g, 5%-EtOAc/hexane) to afford 5-isopropenyl-o-anis-aldehyde, as a yellow oil (2.49 g, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05837711
Source datasetuspto-grants-1998_11
ORD IDord-09d7c67acf754c5591ba49be0fa29d46
Source noteuspto-grants-1998_11