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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942478Generated: November 3, 2026

Diisopropylamine → 6-Bromo-2-fluoro-3-(methoxymethoxy)benzaldehyde

https://huagongshe.com/reaction/1942478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-2-fluoro-1-(methoxymethoxy)benzeneHCID 22032015—
ReactantButyllithiumHCID 178418339—
SolventDimethylformamideHCID 6228—
Product6-Bromo-2-fluoro-3-(methoxymethoxy)benzaldehydeHCID 86656354—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of diisopropylamine (364 μl) in tetrahydrofuran (1 ml) was cooled to −78° C., and thereto was added dropwise n-butyl lithium (0.86 ml, 2.77M hexane solution), and the mixture was stirred at 0° C. for 10 minutes. The reaction mixture was cooled to −78° C., and thereto was added dropwise a solution of 1-bromo-3-fluoro-4-(methoxymethoxy)benzene (470 mg) in tetrahydrofuran (1 ml), and the mixture was stirred for 30 minutes. To the mixture was added dropwise N,N-dimethyl-formamide (210 μl), and the mixture was stirred at room temperature for one hour. To the reaction mixture was added a saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate, washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (48 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389511B2
Source datasetuspto-grants-2013_03
ORD IDord-091abbf7ab8b44cda39210dc24dc45e6
Source noteuspto-grants-2013_03