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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860659Generated: November 3, 2026

Tetrahydrofuran → (3-Fluoro-4-methylphenyl)methanol

https://huagongshe.com/reaction/1860659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-Fluoro-p-anisaldehydeHCID 67696—
ReactantHydrideHCID 166653—
Product(3-Fluoro-4-methylphenyl)methanolHCID 2774590—

Reaction Steps

3-fluoro-p-anisaldehyde (12.5 g, 81.1 mmol) was dissolved in 100 ml THF. Under N2 a solution of diisobutylalumium hydride (100 ml, 1M in THF) was added at 0° C. over 30 min. The reaction was stirred for 30 min and quenched with 250 ml 1 N HCl solution. The mixture was stirred for 15 min and filtered through a short column of Celite®. The aqueous layer was extracted with ethyl acetate. The combined organic layer was dried with MgSO4, and concentrated to give an oil in 11.6 g. This product was used without further purification. NMR spectra of the product were consistent for the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531494B1
Source datasetuspto-grants-2003_03
ORD IDord-f33c24492b35433ab625dc48cb19cbeb
Source noteuspto-grants-2003_03