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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715752Generated: October 29, 2026

Dichloromethane → 4-(1-isobutyl-1H-pyrazol-4-yl)aniline

https://huagongshe.com/reaction/715752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-BromoanilineHCID 7807—
ReactantSodium CarbonateHCID 10340—
Reactant1-Isobutyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2759392—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventMethanol tetrahydrofuran waterHCID 21892291—
Product4-(1-isobutyl-1H-pyrazol-4-yl)anilineHCID 63328393—

Reaction Conditions

Temperature85 °C

Reaction Steps

A suspension of 4-bromoaniline (406 mg, 2.362 mmol), 1-isobutyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (650 mg, 2.60 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane (57.9 mg, 0.071 mmol) and sodium carbonate (526 mg, 4.96 mmol) in a 6:2:1 mixture of tetrahydrofuran/water/methanol (12 ml) in a microwave vial was subjected to three vacuum/nitrogen purge cycles. The vial was sealed and heated in an oil bath at 85° C. overnight. The mixture was dissolved in a mixture of ethyl acetate (45 ml) and water (20 ml), and the separated aqueous layer was extracted with ethyl acetate (20 ml). The combined organic layers were washed with brine (20 ml), dried with magnesium sulfate, filtered and concentrated. Normal phase chromatography provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187472B2
Source datasetuspto-grants-2015_11
ORD IDord-5d78eb3e48f04417a3cc7dc49f97917f
Source noteuspto-grants-2015_11