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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923983Generated: November 2, 2026

Ethylenediamine → Benzyl N-(2-aminoethyl)carbamate

https://huagongshe.com/reaction/1923983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantHCID 22716645HCID 22716645—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductBenzyl N-(2-aminoethyl)carbamateHCID 279425780%

Reaction Steps

To a solution of 2-aminoethylamine LVIII (150 mL; 2.25 mol) in chloroform (1.5 L), cooled to 0° C. was added a solution of carbobenzoxy N-hydroxysuccinimide (112.14 g; 0.45 mol) in water (0.5 L) with vigorously stirring for one hour. The solid was filtered and the solution was washed with brine (3×), once with water and dried over anhydrous MgSO4. The solvent was evaporated under reduced pressure and the residue was purified on a silica gel column (100:1→30:1 DCM:MeOH) to yield benzyl 2-aminoethylcarbamate LIX as a colorless viscous oil (350 g; 1.80 mol; 80% yield). 1H NMR (CDCl3) 2.79-2.83 (m, 2H), 3.21-3.28 (m, 2H), 5.10 (s, 2H), 5.19 (brs, 1H), 7.29-7.34 (m, 1H), 7.35-7.38 (m, 4H); ESIMS found for C10H14N2O2 m/z 195.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178490B2
Source datasetuspto-grants-2012_05
ORD IDord-78f458d1a13443b4ba484f2bf71c2d78
Source noteuspto-grants-2012_05