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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377135Generated: November 1, 2026

Hexane → HCID 68935565, compound

https://huagongshe.com/reaction/2377135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1-Bromo-3,5-dimethoxybenzeneHCID 639187—
ReactantN-Methoxy-N-methylquinoline-6-carboxamideHCID 55211172—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68935565HCID 68935565—

Reaction Steps

To a solution of 1-bromo-3,5-dimethoxy-benzene (2.7 g, 12 mmol) in THF (20 mL) was added a solution of n-butyllitium in hexane (4.5 mL, 2.5 N, 11 mmol) at −78° C. and kept for 20 min. To the mixture was added quinoline-6-carboxylic acid methoxy-methyl-amide (2.2 g, 10 mmol) at −78° C. After 2 h, water (30 mL) was added to the mixture, and the cold bath was removed. The mixture was stirred at room temperature for 20 min. The mixture was extracted with ethyl acetate (2×50 mL). The combined organic layers was washed with sodium hydrogen carbonate (50 mL, sat), brine (50 mL) and dried over magnesium sulfate. Removal of solvent and slurry in ether gave (3,5-dimethoxy-phenyl)-quinolin-6-yl-methanone as a white solid (1.48 g, 50% crude yield). The sample was used in the next step without further purification. 1H NMR (CDCl3) δ 3.84 (s, 6H, 2CH3), 6.70-6.73 (m, 1H, Ar), 6.97 (d, J=2 Hz, 1H, Ar), 7.49 (dd, J=4, 8 Hz, 1H, Ar), 8.17-8.28 (m, 4H, Ar), 9.02-9.04 (m, 1H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468446B2
Source datasetuspto-grants-2008_12
ORD IDord-92650f9afe254f5bbf380cfd9a058541
Source noteuspto-grants-2008_12