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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783992Generated: October 30, 2026

Hydrochloric Acid → 4-(4-tert-Butylpiperazin-1-yl)aniline

https://huagongshe.com/reaction/1783992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantStannous chloride dihydrateHCID 61436—
Reactant1-Tert-butyl-4-(4-nitrophenyl)piperazineHCID 57444158—
SolventMethanolHCID 887—
Product4-(4-tert-Butylpiperazin-1-yl)anilineHCID 24279182100%

Reaction Conditions

Temperature40 °C

Reaction Steps

1-tert-Butyl-4-(4-nitro-phenyl)-piperazine (348 mg, 1.32 mmol) is dissolved in MeOH (10 mL) and tin (II) dichloride dihydrate (1.08 g, 4.79 mmol) is added. The mixture is cooled using a water bath and conc. HCl is added (3 mL). The reaction is stirred at 40° C. overnight. After removing the methanol, the resultant solution is basified using conc. NaOH (pH 11). The water phase is extracted with diethyl ether (3×) and the organic layers combined, dried over MgSO4, filtered, concentrated in vacuo to afford the title compound (308 mg, 99%) which is used in the next step without further purification. LCMS: Rt 2.16 min (87%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501411B2
Source datasetuspto-grants-2009_03
ORD IDord-fbaea089ba5241909d095e7297b4658b
Source noteuspto-grants-2009_03