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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257849Generated: October 26, 2026

O-Xylene → 1,2-Dihydro-4-[(4-ethylaminophenyl)methyl]-5-(trifluoromethyl)-3H-pyrazol-3-one

https://huagongshe.com/reaction/257849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
ReactantAcetamide, N-(4-(chloromethyl)phenyl)-HCID 148705—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant4-[(4-acetamidophenyl)methyl]-5-(trifluoromethyl)-3H-pyrazol-3-oneHCID 19782087—
SolventTetrahydrofuranHCID 8028—
Product1,2-Dihydro-4-[(4-ethylaminophenyl)methyl]-5-(trifluoromethyl)-3H-pyrazol-3-oneHCID 10779467—

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of borane-THF complex (188 mL, 1M solution in tetrahydrofuran), diluted with 200 mL tetrahydrofuran, was cooled to -30° C. under N2 atmosphere. A solution of 4-[(4-acetamidophenyl)methyl]-5-(trifluoromethyl)-3H-pyrazol-3-one (6 g, prepared as in Example 1 (except that 4-acetamidobenzylchloride was reacted with the β-keto ester anion in refluxing xylene) in tetrahydrofuran (300 mL) was added over 0.75 hours and the mixture allowed to warm gradually to ambient temperature with stirring for 15 hours. The reaction mixture was refluxed for 3 hours, then cooled in ice and quenched with aqueous sodium hydroxide solution (24 mL, 2.5N). The mixture was stirred for 2 hours at ice temperature and 15 hours at room temperature. Volatile materials were removed in vacuo on the rotary evaporator. The residue was solubilized in distilled water, brought to pH 7 with dilute, aqueous HCl solution and extracted with ethyl acetate. The extracts were washed with saturated brine solution, dried over MgSO4, filtered and concentrated. The residue was dissolved in isopropyl alcohol saturated with anhydrous HCl and cooled in ice. The precipitate was collected on a suction funnel and dried under vacuum (abderhalden apparatus) to afford the title compound as a pale yellow glass; sinters at 104° C., liquefies 169°-171° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05264451
Source datasetuspto-grants-1993_11
ORD IDord-918b29f42e5a4b4b96c4a8058e47e77e
Source noteuspto-grants-1993_11