HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → 1,3-Bis(cyclohexylmethyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Cyclohexanemethylamine | HCID 76688 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,3-Bis(cyclohexylmethyl)urea | HCID 231515 | 95% |
Reaction Steps
A mixture of cyclohexanemethylamine (Aldrich, 68.66 g) and 5 N sodium hydroxide (Fisher, 200 ml) was stirred vigorously with cooling (−10° C.) while a solution of phosgene (30.0 g) in toluene (600 ml) was added rapidly. After stirring for 20 minutes, the resulting mixture was filtered and the precipitated solid was washed with water (˜1500 ml) and dried at 67 Pa (0.5 Torr) to give 1,3-bis(cyclohexylmethyl)urea as white powder (72.72 g, 95%), m.p. 150-152° C.; 1H-NMR (DMSO-d6) δ: 5.74 (br t, J=5.8 Hz, 2, 2 NH), 2.81 (t, J=6.3 Hz, 4, 2 NCH2), 1.62, 1.25, and 0.85 (all m, 22, 2 cyclohexyl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06355646B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-da94a1eb9a9e4c98b4951d153e29cb08 |
| Source note | uspto-grants-2002_03 |