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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378239Generated: October 29, 2026

4-bromo-N,N-dimethylaniline → HCID 11333766, compound

https://huagongshe.com/reaction/378239

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-bromo-N,N-dimethylanilineHCID 11465—
ReactantN-Methoxy-N-methylheptanamideHCID 13642088—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11333766HCID 1133376648.2%

Reaction Steps

n-Butyllithium (2.5 M in hexanes, 51 mL, 127 mmol) was added dropwise to 4-bromo-N,N-dimethylaniline (23.1 g, 115 mmol, Aldrich Chemical Co.) in anhydrous THF at -78° C. After 10 min. a solution of N-methyl-N-methoxyheptanamide (10.0 g, 57.7 mmol) in 20 mL THF was added dropwise via canula. The reaction was allowed to proceed 1 hr., then quenched with 1 N aq. HCl and carefully poured into sat. NaHCO3. The aqueous layer was extracted with ethyl ether, and the combined organic fraction was washed with water, brine, dried (MgSO4), and concentrated in vacuo. Flash chromatography (15% EtOAc/hexanes) yielded 1-(4-dimethylaminophenyl)heptan-1-one as a yellow solid (6.49 g, 48%). MS 234 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030969
Source datasetuspto-grants-2000_02
ORD IDord-03151e11241f452182984598ce47b026
Source noteuspto-grants-2000_02