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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171609Generated: October 30, 2026

Tetrabutylammonium Fluoride → HCID 71239368, compound

https://huagongshe.com/reaction/2171609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 131732948HCID 131732948—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 71239368HCID 71239368—

Reaction Steps

To a stirred solution of 4-((3S,3aR,4S)-4-((tert-butyldimethylsilyl)oxy)-3-(cyclopropylmethoxy)-3a,4,5,6-tetrahydro-3H-pyrrolo[1,2-b]pyrazol-2-yl)-2-chloro-3-methylbenzonitrile (60 mg, 0.13 mmol) in THF (2 mL) at 0° C. was added TBAF (0.26 mL, 0.26 mmol, 1M Solution in THF) and stirred for 1 h at room temperature. Once the starting material had disappeared (monitored by TLC), reaction mixture was diluted with ethyl acetate. Organic layer was washed with water, brine, dried over Na2SO4 and concentrated. Crude product was purified by preparative TLC method (50% EtOAc in hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051326B2
Source datasetuspto-grants-2015_06
ORD IDord-045359a429c945c7bc6f6c6dab6ac22b
Source noteuspto-grants-2015_06