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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890815Generated: October 29, 2026

Tetrabutylammonium Fluoride → ethyl 5-(3-hydroxypropyl)-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/890815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-1H-pyrazole-3-carboxylic Acid Ethyl EsterHCID 53952793—
SolventTetrahydrofuranHCID 8028—
Productethyl 5-(3-hydroxypropyl)-1H-pyrazole-3-carboxylateHCID 5451132279.3%

Reaction Steps

A solution of 5-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-1H-pyrazole-3-carboxylic acid ethyl ester (327 mg, 1.05 mmol) and tetrabutylammonium fluoride (288 mg, 1.10 mmol) in THF (50 mL) was stirred at room temperature for 1 h. The reaction mixture was concentrated in vacuo. Flash chromatography (EtOAc to EtOAc:MeOH 19:1) provided the title alcohol (165 mg). 1H NMR (400 MHz, CDCl3) δ 6.58 (s, 1H), 4.35 (q, 2H), 3.71 (t, 2H), 2.84 (t, 2H), 1.91 (m, 2H), 1.36 (t, 3H); MS 199 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06998423B2
Source datasetuspto-grants-2006_02
ORD IDord-d0315845671843139e54333f4b1e0696
Source noteuspto-grants-2006_02