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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226440Generated: October 30, 2026

1,2-Ethanediamine, N1,N1-bis(1-methylethyl)- → HCID 86748144, compound

https://huagongshe.com/reaction/2226440

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Ethanediamine, N1,N1-bis(1-methylethyl)-HCID 8459—
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 86748144HCID 86748144—

Reaction Conditions

Temperature0 °C

Reaction Steps

N,N-Diisopropyl-ethylenediamine (4.94 gm, 0.034 mol) was dissolved in CH2Cl2 (20 mL) and cooled to 0° C. under nitrogen. Triethylamine (4.7 mL) and benzyloxycarbonyl chloride (4.9 mL) were then added and the mixture was stirred overnight while being allowed to reach room temperature. The mixture was then poured into Et2O (250 mL) and K2CO3 was added. This mixture was then washed successively with H2O and brine and the pooled aqueous layers were back-extracted with Et2O. The pooled organic layers were dried over Na2SO4, filtered and evaporated to dryness. This crude reaction product was then purified on a silica gel column using initially EtOAc/hexane (1:1) as eluent followed by MeOH/EtOAc (3:7) containing 2% Et3N to afford 2.9 gm of the title compound suitable for use in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348953
Source datasetuspto-grants-1994_09
ORD IDord-61cd80437f27453ebe5bbffeea686825
Source noteuspto-grants-1994_09