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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174832Generated: October 26, 2026

Acetic Acid → 4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-benzoic acid

https://huagongshe.com/reaction/1174832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-Hydrazinobenzoic acidHCID 12089—
ReactantPentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
SolventTetrahydrofuran ethanolHCID 21873804—
Product4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-benzoic acidHCID 97468899%

Reaction Steps

A mixture of 4,4-dimethyl-3-oxo-pentanenitrile (4.52 g, 36.15 mmol), 4-hydrazinobenzoic acid (5.00 g, 32.86 mmol), and acetic acid (2 mL) in EtOH/THF (1:1) was refluxed for 16 h. After cooling, the solvent was concentrated at reduced pressure, and the crude was re-dissolved in EtOAc. The organic layer was washed with aqueous saturated Na2CO3 solution and brine, dried over MgSO4, filtered, and concentrated to half its volume. The resulting residue was filtered, and the solids were washed with cold EtOAc and dried under high vacuum to afford the title compound as a white solid (8.4 g, 99%). 1H-NMR (DMSO-d6) δ 12.91 (s, 1H), 7.99 (d, J=6.0 Hz, 2H), 7.75 (d, J=9.0 Hz, 2H), 5.42 (s, 1H), 5.39 (s, 2H), 1.21 (s, 9H); MS LC-MS [M+H]+=260, RT=1.83 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838524B2
Source datasetuspto-grants-2010_11
ORD IDord-ee33ca7f0c31475db118e4b5cef513e0
Source noteuspto-grants-2010_11