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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378274Generated: November 1, 2026

Hexane → HCID 69205838, compound

https://huagongshe.com/reaction/2378274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant3-(1H-Pyrrol-1-yl)benzaldehydeHCID 2776528—
Reactant4-Bromo-2-ethoxy-1-methoxybenzeneHCID 21772690—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69205838HCID 69205838101.3%

Reaction Steps

To a solution of 4-bromo-2-ethoxy-1-methoxy-benzene (1.5 g, 6.5 mmol) in THF (30 mL) was added a solution of n-butyllitium in hexane (2.4 mL, 2.5 N, 6.0 mmol) at −78° C. and kept for 20 min. To the mixture was added 3-pyrrol-1-yl-benzaldehyde (1.0 g, 5.8 mmol) at −78° C. After 18 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 HCl (0.5 N, 50 mL), sodium hydrogen carbonate (50 mL, sat), brine (50 mL) and dried over magnesium sulfate. Removal of solvent gave (3-ethoxy-4-methoxy-phenyl)-(3-pyrrol-1-yl-phenyl)-methanol (1.9 g, 100% crude yield). The sample was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470723B2
Source datasetuspto-grants-2008_12
ORD IDord-ed6c95cbcb3547ff9199afcefc4a0677
Source noteuspto-grants-2008_12