Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042092Generated: November 2, 2026

Lithium Hydroxide → 3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazole-5-carboxylic acid

https://huagongshe.com/reaction/2042092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactantethyl 3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazole-5-carboxylateHCID 67251871—
SolventDioxane ethanol waterHCID 69104347—
Product3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazole-5-carboxylic acidHCID 6725310594%

Reaction Steps

Lithium hydroxide (62 mg, 2.6 mmol) was added to a solution of ethyl 3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazole-5-carboxylate (0.21 g, 0.65 mmol) in dioxane-H2O-EtOH (1:1:1, 6 mL). The reaction mixture was stirred overnight at RT. The solution was concentrated and the residue was dissolved in H2O (2 mL). 3M HCl was added and the precipitate was collected by filtration and washed with water. The solid was dried under vacuum to obtain 3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazole-5-carboxylic acid (0.18 g, 94% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 8.96 (dd, J=2.0, 4.0 Hz, 1H), 8.47 (dd, J=1.2, 8.4 Hz, 1H), 8.09 (m, 1H), 8.06 (s, 1H), 7.82 (dd, J=2.8, 9.2 Hz, 1H), 7.61 (dd, J=4.8, 8.8 Hz, 1H), 7.01 (s, 1H), 1.33 (s, 9H); MS (ESI) m/z: 296.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586565B2
Source datasetuspto-grants-2013_11
ORD IDord-62f2d7b6929e415fb621f54f7a13ca0f
Source noteuspto-grants-2013_11