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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746771Generated: October 25, 2026

Dimethylformamide → 6-Bromo-2,4-difluoro-3-methoxybenzaldehyde

https://huagongshe.com/reaction/746771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylamineHCID 7912—
ReactantLithium diisopropylamideHCID 2724682—
Reactant4-Bromo-2,6-difluoroanisoleHCID 2773287—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-2,4-difluoro-3-methoxybenzaldehydeHCID 86613168—

Reaction Conditions

Temperature0 °C

Reaction Steps

Add n-butyl lithium 1.6N (22 ml, 35.2 mmol) to diisopropylamine (4.8 ml, 34.2 mmol) in anhydrous THF (7 ml) at 0° C. Stir the resulting yellow solution for 30 min at 0° C. Add this LDA solution dropwise via canula to a solution of 5-bromo-1,3-difluoro-2-methoxybenzene (5.83 g, 26.17 mmol) in anhydrous THF (40 ml) at −78° C. over 40 min. Stir the resulting bright yellow solution for 50 min at −78° C. Add anhydrous DMF (2.7 ml, 34.8 mmol) and stir the mixture for 1.5 h at −78° C. Quench the mixture with dilute sulfuric acid and extract the product with EtOAc (×3). Wash the combined organic layers with water (×3), saturated aq. sodium chloride and dry over anhydrous sodium sulfate. Filter and concentrate to yield the crude product. Purification by flash chromatography (Silica gel-hexane/EtOAc) yields the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393868B2
Source datasetuspto-grants-2008_07
ORD IDord-7fc61f9df81040f2be821a7b4c31d756
Source noteuspto-grants-2008_07