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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361443Generated: October 26, 2026

Acetone → 2-(4-Bromo-3,5-dimethyl-1H-pyrazol-1-yl)-2-methylpropanoic acid

https://huagongshe.com/reaction/1361443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantChlorobutanolHCID 5977—
ReactantSodium HydroxideHCID 14798—
Reactant4-bromo-3,5-dimethyl-1H-pyrazoleHCID 76937—
Product2-(4-Bromo-3,5-dimethyl-1H-pyrazol-1-yl)-2-methylpropanoic acidHCID 66628195—

Reaction Steps

To a cold (0° C.), well stirred suspension of NaOH (1.6 g, 40 mmoles) and 4-bromo-3,5-dimethylpyrazole (1.75 g, 10 mmoles) in acetone (100 mL), was added 2-(trichloromethyl)-propan-2-ol (3.54 g, 20 mmoles)/portion-wise over 1 hour. The mixture was allowed to warm to room temperature overnight. The solvent was evaporated under reduced pressure. The residue was dissolved in water (100 mL) and washed with ether (50 mL). The aqueous phase was separated and acidified with conc. HCl to pH=3. The mixture was extracted with CH2Cl2 (3×50 mL) and the combined organics dried over Na2SO4. A colorless oil was obtained after the removal of the solvent under reduced pressure. MS(DCI+) m/z 263 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880001B2
Source datasetuspto-grants-2011_02
ORD IDord-0232966b45034098a93dbc565d25e2e2
Source noteuspto-grants-2011_02