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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836550Generated: November 1, 2026

Tetrabutylammonium Fluoride Trihydrate → {4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]phenyl}methanol

https://huagongshe.com/reaction/1836550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium Fluoride TrihydrateHCID 11726816—
Reactant({4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}oxy)(tertbutyl)dimethylsilaneHCID 23499610—
SolventTetrahydrofuranHCID 8028—
Product{4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]phenyl}methanolHCID 23499600—

Reaction Steps

3.4 g (6.99 mmol) of ({4-(benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}oxy)(tertbutyl)dimethylsilane (Example IV) are dissolved in 10 ml of tetrahydrofuran. At room temperature, 7.68 mmol of tetrabutylammonium fluoride trihydrate (1-molar solution in THF) are added. The mixture is stirred at room temperature overnight. The solvent is then removed under reduced pressure and the product is purified by chromatography on silica gel 60 (mobile phase: cyclohexane/ethyl acetate 3:2). This gives 2.1 g (81% of theory) of {4-(benzyloxy)-3-[(4-fluorophenyl)sulphonyl]phenyl}methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777442B2
Source datasetuspto-grants-2004_08
ORD IDord-c8c7f73d58534247b24d15a4407f9d41
Source noteuspto-grants-2004_08