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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410287Generated: November 2, 2026

Ethanol → tert-butyl N-{[4-(aminomethyl)phenyl]methyl}carbamate

https://huagongshe.com/reaction/1410287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1,4-BenzenedimethanamineHCID 68315—
ReactantHCID 53420676HCID 53420676—
Producttert-butyl N-{[4-(aminomethyl)phenyl]methyl}carbamateHCID 3354775—

Reaction Steps

Tert-butylphenyl carbonate (2.7 mL, 14.7 mmol) was added dropwise to a solution of p-xylylenediamine (2 g, 14.7 mmol) in ethanol (20 mL) at 80° C. The reaction mixture was refluxed overnight. The solution was then cooled to room temperature and any solids were removed, which leaves a yellow solution. The solution was then concentrated to 10 mL and diluted with water (60 mL). The solution pH was adjusted to 3 with 2M HCl followed by an extraction with dichloromethane (3×75 mL). The water solution pH was then adjusted to pH 12 followed by extraction with dichloromethane (3×75 mL). The organic solutions were combined and washed with sodium bicarbonate (2×75 mL), dried with sodium sulfate, and concentrated down to a white solid. Characterization matches previously published literature (M. A. Ghanem, et al., “Covalent modification of glassy carbon surface with organic redox probes through diamine linkers using electrochemical and solid-phase synthesis methodologies”, Journal of Materials Chemistry, (2008), 18(41), pg 4917-4927).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921426B2
Source datasetuspto-grants-2014_12
ORD IDord-5bfb875b4e83407fa5a4c9eefae31918
Source noteuspto-grants-2014_12