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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Ethanediamine, N1,N1-bis(1-methylethyl)- | HCID 8459 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86748144 | HCID 86748144 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05348953 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-61cd80437f27453ebe5bbffeea686825 |
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| Source note | uspto-grants-1994_09 |
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