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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270114Generated: November 4, 2026

Tetrabutylammonium Fluoride → 1-(7-Methoxybenzofuran-2-yl)-butane-1,4-diol

https://huagongshe.com/reaction/2270114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-(tert-Butyldimethylsilanyloxy)-1-(7-methoxybenzofuran-2-yl)-butan-1-olHCID 18423652—
Product1-(7-Methoxybenzofuran-2-yl)-butane-1,4-diolHCID 1842364786.8%

Reaction Steps

Tetrabutylammonium fluoride (12 ml, 1M in tetrahydrofuran) was added to a stirred solution of 4-(tert-butyldimethylsilanyloxy)-1-(7-methoxybenzofuran-2-yl)-butan-1-ol (4 g) in tetrahdrofuran (50 ml) at 0° C. After stirring cooled for 2 hours the reaction was warmed to room temperature and allowed to stir for a further 1 hour. The solvent was removed in vacuo and the residue partitioned between ethyl acetate (100 ml) and water (50 ml). The organic extract was dried over magnesium sulphate, filtered and preadsorbed onto silica. Purification by column chromatography on silica eluting with ethyl acetate yielded the title compound as a tan oil (2.34 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331556B2
Source datasetuspto-grants-2001_12
ORD IDord-8cf74de0831b4279b132d992b099277d
Source noteuspto-grants-2001_12