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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62773Generated: October 29, 2026

Tetrabutylammonium Fluoride → (4-Fluoro-3,5-diisopropoxyphenyl)methanol

https://huagongshe.com/reaction/62773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactanttert-Butyl(4-fluoro-3,5-diisopropoxybenzyloxy)dimethylsilaneHCID 67041823—
SolventTetrahydrofuranHCID 8028—
Product(4-Fluoro-3,5-diisopropoxyphenyl)methanolHCID 67041705116.8%

Reaction Steps

TBAF (1M in THF) (1.35 mL, 1.35 mmol) was added to a solution of tert-butyl(4-fluoro-3,5-diisopropoxybenzyloxy)dimethylsilane (6) (600 mg, 1.35 mmol) in THF at 0° C. and the mixture was stirred at this temperature for 1 h. The mixture was partitioned between NH4Cl (satd. aq.) (50 mL) and EtOAc (100 mL). The phases were separated and the organic solution was washed with brine (50 mL), then dried over MgSO4 and filtered. The solvent was removed in vacuo and the residue was purified by silica gel chromatography (40 g, 0-50% EtOAc in isohexane) to afford (4-fluoro-3,5-diisopropoxyphenyl)methanol (7) (382 mg, 100%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447028B2
Source datasetuspto-grants-2016_09
ORD IDord-8ac8f2fcf53c4b29a080071df32350e6
Source noteuspto-grants-2016_09