Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171600Generated: October 31, 2026

Tetrabutylammonium Fluoride → HCID 71239141, compound

https://huagongshe.com/reaction/2171600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 131732945HCID 131732945—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 71239141HCID 71239141—

Reaction Steps

To a solution of 4-((3S,3aR,4S)-4-(tert-butyldimethylsilyloxy)-3-(tetrahydro-2H-pyran-2-yloxy)-3a,4,5,6-tetrahydro-3H-pyrrolo[1,2-b]pyrazol-2-yl)-2-chloro-3-methylbenzonitrile (120 mg, 0.245 mmol) in THF (2 mL) at 0° C. was added tetrabutylammonium fluoride (0.49 mL, 0.490 mmol, 1M solution in THF) and the reaction mixture was stirred at room temperature for 3 h. Once the starting material had disappeared (monitored by TLC), it was diluted with ethyl acetate and the organic layer was washed with water, brine, dried over Na2SO4 and concentrated. Purification of crude by column chromatography over silica gel using 30% EtOAc in hexane provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051326B2
Source datasetuspto-grants-2015_06
ORD IDord-346c47f84ffa4c2bb51e24fcf2f4f3dd
Source noteuspto-grants-2015_06