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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396501Generated: October 31, 2026

Tetrabutylammonium Fluoride → HCID 178469378, compound

https://huagongshe.com/reaction/1396501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactantethyl 1-{2-[(tert-butoxycarbonyl)amino]ethyl}-3-{[tert-butyl(dimethyl)silyl]oxy}-1H-pyrazole-5-carboxylateHCID 86706487—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178469378HCID 17846937883%

Reaction Steps

A 1 M solution of tetrabutylammonium fluoride in THF (20.1 mL, 20.1 mmol) was added to a stirred solution of ethyl 1-{2-[(tert-butoxycarbonyl)amino]ethyl}-3-{[tert-butyl(dimethyl)silyl]oxy}-1H-pyrazole-5-carboxylate (5.54 g, 13.4 mmol) in THF (45 mL). The mixture was stirred at room temperature for 16 hours, diluted with water and extracted with AcOEt. The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo to yield ethyl 1-{2-[(tert-butoxycarbonyl)amino]ethyl}-3-hydroxy-1H-pyrazole-5-carboxylate (3.32 g, 83% yield) as a white solid, that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901125B2
Source datasetuspto-grants-2014_12
ORD IDord-3db36c3d6a51490981d3630a263ab9cd
Source noteuspto-grants-2014_12