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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377129Generated: October 30, 2026

Hexane → 3-Ethoxy-4-methoxybenzaldehyde

https://huagongshe.com/reaction/2377129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant5-Bromo-2,3-dihydro-1-benzofuranHCID 2776159—
Reactant3-ethoxy-N,4-dimethoxy-N-methylbenzamideHCID 21311018—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventTetrahydrofuranHCID 8028—
Product3-Ethoxy-4-methoxybenzaldehydeHCID 244728148.4%

Reaction Steps

To a solution of 5-bromo-2,3-dihydro-benzofuran (1.0 g, 5.0 mmol) in THF (10 mL) was added a solution of n-butyllitium in hexane (1.8 mL, 2.5 N, 4.5 mmol) at −78° C. and kept for 20 min. To the mixture was added a solution of 3-ethoxy-4,N-dimethoxy-N-methyl-benzamide (1.1 g, 4.6 mmol) in THF (10 mL) at −78° C. After 30 min, isopropanol (1 mL) and water (10 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 (50 mL) and water (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL). The combined organic layers was washed with HCl (1N, 50 mL), water (50 mL), brine (50 mL) and dried over MgSO4. Removal of solvent and gave 2,3-dihydro-benzofuran-5-yl)-(3-ethoxy-4-methoxy-phenyl)-methanone as an oil (1.23 g, 92% yield). The oil was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468446B2
Source datasetuspto-grants-2008_12
ORD IDord-a0151f278c1e44da8c12d347ae4fbfca
Source noteuspto-grants-2008_12