HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl isocyanate → HCID 47448393, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86760688 | HCID 86760688 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 47448393 | HCID 47448393 | 98.6% |
Reaction Steps
N-Ethyl-N′-(3-nitrobenzyl)urea 3-Nitrobenzylamine hydrochloride (754 mg, 4.0 mmol) and triethylamine (404 mg, 4 mmol) were stirred in THF (10 ml) for 15 min in an ice bath. Ethylisocyanate (335 μl, 4.23 mmol) was added dropwise to the solution and the reaction allowed to stand at room temperature for 2 h after addition was complete. The reaction was partitioned between ethyl acetate (30 ml) and water (30 ml). The organic phase was washed with water, brine and dried (sodium sulphate). The solvent was evaporated under vacuum to give N-ethyl-N′-(3-nitrobenzyl)urea (880 mg). Rf; DCM/methanol (10:1) 0.40.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07384963B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-315c8e9751e847c48e13394ebe10f731 |
| Source note | uspto-grants-2008_06 |