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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378269Generated: November 2, 2026

Hexane → HCID 69205124, compound

https://huagongshe.com/reaction/2378269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant4-Bromo-2-ethoxy-1-methoxybenzeneHCID 21772690—
ReactantHCID 25130165HCID 25130165—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69205124HCID 6920512444.2%

Reaction Steps

To a solution of 4-bromo-2-ethoxy-1-methoxy-benzene (0.67 g, 2.9 mmol) in THF (10 mL) was added a solution of n-butyllitium in hexane (1.1 mL, 2.5 N, 2.8 mmol) at −78° C. and kept for 20 min. To the mixture was added a solution of 3-fluoro-4,N-dimethoxy-N-methyl-benzamide (0.56 g, 2.6 mmol) in THF (4 mL) at −78° C. After 2 h, isopropanol (1 mL) and 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 HCl (0.5 N, 50 mL), sodium hydrogen carbonate (50 mL, sat), brine (50 mL) and dried over magnesium sulfate. Removal of solvent and chromatography (Silica Gel) gave (3-ethoxy-4-methoxy-phenyl) -(3-fluoro-4-methoxy-phenyl)-methanone (350 mg, 44% yield): 1H NMR (DMSO-d6) δ 1.49 (t, J=7 Hz, 3H, 2CH3), 3.96 (s, 3H, CH3), 3.98 (s, 3H, CH3), 4.16 (q, J=7 Hz, 2H, CH2), 6.90 (d, J=8 Hz, 1H, Ar), 7.02 (t, J=9 Hz, 1H, Ar), 7.35 (dd, J=2, 8 Hz, 1H, Ar), 7.41 (d, J=2 Hz, 1H, Ar), 7.55-7.62 (m, 2H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470723B2
Source datasetuspto-grants-2008_12
ORD IDord-6c056e3b4e5746e6868975e23f2c2418
Source noteuspto-grants-2008_12