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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1,4-Benzenedimethanamine | HCID 68315 | — |
| Reactant | HCID 53420676 | HCID 53420676 | — |
| Product | tert-butyl N-{[4-(aminomethyl)phenyl]methyl}carbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921426B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-5bfb875b4e83407fa5a4c9eefae31918 |
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| Source note | uspto-grants-2014_12 |
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