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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027635Generated: November 2, 2026

Ethylenediamine → Benzyl N-(2-aminoethyl)carbamate

https://huagongshe.com/reaction/1027635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantMethanesulfonic AcidHCID 6395—
ReactantBenzyl chloroformateHCID 10387—
ReactantHCID 178476685HCID 178476685—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductBenzyl N-(2-aminoethyl)carbamateHCID 279425751%

Reaction Steps

Ethylenediamine (1.0 g, 16.7 mmol) is dissolved in water (3.0 mL) containing bromoaresal green as an indicator. Methane sulfonic acid (2.8 g, 31 mmol) in water (3.0 ml) was added until a blue to pale yellow color transition is just achieved. The solution was diluted with ethanol (8.0 mL) and vigorously stirred. To the mixture was added the solution of Cbz-Cl (2.8 g, 16.7 mmol) in dimethoxyethane (4 mL) and 50% w/v aqueous AcOK (10 mL) at 20° C. simultaneously to maintain the pale yellow-green color of the indicator. After the additions are complete the mixture was stirred (RT, 1 h) and concentrated at low temperature under vacuum to removed the volatiles. The residue was shaken with water (20 mL) and filtered. The filtrate was then washed with toluene (3×50 mL), basified with excess 40% aqueous NaOH and extracted with toluene (3×50 mL). The organic layer was washed with brine (50 mL), dried over Na2SO4 and evaporated to give benzyl 2-aminoethylcarbamate as an oil (1.65 g, 51%). Mass calculated for C10H14N2O2=194.23. found: [M−H]+=193.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735379B2
Source datasetuspto-grants-2014_05
ORD IDord-f0ac3fec09e1410597ec6f4fe75bbec2
Source noteuspto-grants-2014_05