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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499198Generated: October 31, 2026

Sodium Bicarbonate → tert-Butyl 4-((4-aminophenyl)methyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/499198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1-Boc-4-(4-Nitrobenzyl)piperazineHCID 23506946—
ReactantTin tetrachloride dihydrateHCID 85782573—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-((4-aminophenyl)methyl)piperazine-1-carboxylateHCID 1204500189%

Reaction Steps

4-(4-Nitro-benzyl)-piperazin-1-yl carboxylic acid tert-butyl ester (769 mg, 2.4 mmol) and tin chloride dihydrate (2.70 g, 12 mmol) are suspended in ethyl acetate (20 mL) and stirred at room temperature overnight. Then, saturated aqueous solution of sodium bicarbonate (20 mL) is added and vigorously stirred for 1 hour. Solids are removed by filtration and the organic layer of the filtrate is separated and washed with water (20 mL). The organic phase is dried over anhydrous magnesium sulfate and concentrated to give a white solid (620 mg, 89% yield, ES+(m/z) 293 [M+H]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767674B2
Source datasetuspto-grants-2010_08
ORD IDord-22a6201100424ded8c68ca25f011162c
Source noteuspto-grants-2010_08