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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354977Generated: November 1, 2026

Benzocaine → Ethyl 4-((3-aminophenyl)amino)benzoate

https://huagongshe.com/reaction/1354977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzocaineHCID 2337—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BromoanilineHCID 11562—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductEthyl 4-((3-aminophenyl)amino)benzoateHCID 2110613280.4%

Reaction Steps

An oven-dried resealable schlenk tube containing a stir bar was charged with Pd2(dba)3 (4.6 mg, 0.005 mmol), 2-ditbutylphosphino-2′,4′,6′-triisopropylbiphenyl (17.0 mg, 0.04 mmol), ethyl 4-aminobenzoate (125 mg, 0.75 mmol) and K2CO3 (173 mg, 1.25 mmol). The tube was capped with a rubber septum, evacuated and backfilled with argon. 3-Bromoaniline (56 μL, 0.5 mmol) and tbutanol (1 mL) were added through the septum via syringe. The septum was replaced with a Teflon screw cap. The schlenk tube was sealed and put into a pre-heated oil bath at 80° C. The reaction mixture was stirred for 11 h, allowed to cool down to room temperature and filtered through celite with ethyl acetate. The filtrate was concentrated under reduced pressure. Chromatography on silica gel column with 4:1 hexane:ethyl acetate gave 103 mg (80%) of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223879B2
Source datasetuspto-grants-2007_05
ORD IDord-8701cd6c6c1a41afa7ee7824b3af22b0
Source noteuspto-grants-2007_05