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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571721Generated: October 30, 2026

Tetrabutylammonium Fluoride → HCID 178469378, compound

https://huagongshe.com/reaction/571721

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 numberUS09029366B2
Source datasetuspto-grants-2015_05
ORD IDord-b5e03febe79d4ab9abdf793e71ff68b5
Source noteuspto-grants-2015_05