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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585649Generated: October 25, 2026

Hydrochloric Acid → HCID 22337772, compound

https://huagongshe.com/reaction/585649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant3-Methoxycyclopent-2-en-1-oneHCID 643476—
Reactant1-Bromo-2,4-bis(methoxymethoxy)benzeneHCID 11391754—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22337772HCID 2233777213%

Reaction Conditions

Temperature-78 °C

Reaction Steps

1,3-Bis(methoxymethoxy)-4-bromobenzene (1.0 g) was dissolved in THF (20 ml) and cooled to −78° C. under argon. N,N,N′,N′-Tetramethylethylene diamine was added followed by dropwise addition of n-BuLi (3.4 ml of a 2.2M solution in hexanes) over 10 mins. After stirring at −78° C. for 1 hr, a solution of 3-methoxy-2-cyclopentene-1-one (605 mg) in THF (5 ml) was added slowly. The reaction mixture was stirred at −78° C. for 1 hr before warming to 0° C. 1M HCl (20 ml) was added, and after 10 min the mixture was extracted with ethyl acetate (2×50 ml). The combined organic phases were washed with brine (30 ml), dried over magnesium sulfate, and concentrated in vacuo. The crude residue was purified by flash column chromatography (SiO2, ethyl acetate/petrol, 1:1 v/v) to furnish the title compound as yellow oil (128 mg, 13%); m/z (ES+) 279 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933319B2
Source datasetuspto-grants-2005_08
ORD IDord-57bf4e4daa954afbafb517e27cf3bdb7
Source noteuspto-grants-2005_08