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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378271Generated: October 30, 2026

Hexane → (3,5-Dimethoxy-phenyl)-(3-fluoro-4-methoxy-phenyl)-methanol

https://huagongshe.com/reaction/2378271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant3-Fluoro-p-anisaldehydeHCID 67696—
Reactant1-Bromo-3,5-dimethoxybenzeneHCID 639187—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(3,5-Dimethoxy-phenyl)-(3-fluoro-4-methoxy-phenyl)-methanolHCID 61080527105.8%

Reaction Steps

To a solution of 1-bromo-3,5-dimethoxy-benzene (5.0 g, 23.1 mmol) in THF (50 mL) was added a solution of n-butyllitium in hexane (8.7 mL, 2.5 N, 22 mmol) at −78° C. and kept for 20 min. To the mixture was added 3-fluoro-4-methoxy-benzaldehyde (3.0 g, 19.4 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 (3,5-dimethoxy-phenyl)-(3-fluoro-4-methoxy-phenyl)-methanol (6 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-3939341247d54a1ca1fe977f74ba2855
Source noteuspto-grants-2008_12