Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537683Generated: October 25, 2026

1,2-Dimethoxyethane → 9-(5-Bromo-2-ethylphenyl)-3-oxaspiro[5.5]undecane-8,10-dione

https://huagongshe.com/reaction/537683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantIodine, ion (I1+)HCID 3715291—
Reactant2-Ethyl-5-bromophenylboronic acidHCID 59445941—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product9-(5-Bromo-2-ethylphenyl)-3-oxaspiro[5.5]undecane-8,10-dioneHCID 66679999—

Reaction Conditions

Temperature50 °C

Reaction Steps

A portion of the iodonium ylide (2.0 g, 5.21 mmol) is added to a mixture of 2-ethyl-5-bromophenylboronic acid (1.43 g, 6.25 mmol), palladium(II) acetate (59 mg, 0.26 mmol) and lithium hydroxide monohydrate (0.656 g, 15.6 mmol) in 1,2-dimethoxyethane (40 ml) and water (10 ml), and the mixture is heated at 50° C. for 6 hours, and then allowed to stand at room temperature overnight. The mixture is filtered through diatomaceous earth, washing the filter cake with water (50 ml) and ethyl acetate (50 ml). The organic phase is discarded. The aqueous phase is acidified to pH2 by addition of concentrated hydrochloric acid, and then extracted with ethyl acetate. The organic extract is dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 9-(5-bromo-2-ethylphenyl)-3-oxaspiro[5.5]undecane-8,10-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865623B2
Source datasetuspto-grants-2014_10
ORD IDord-145deb73b74741cb952ea9c9df55a26f
Source noteuspto-grants-2014_10