HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetramethylurea → HCID 18952293, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetramethylurea | HCID 12437 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | 2-Morpholinoaniline | HCID 735756 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18952293 | HCID 18952293 | — |
Reaction Steps
Reaction of tetramethylurea (10.4 g, 10.7 ml) in dry benzene (80 ml) with 4-(2-aminophenyl)morpholine (10.2 g) in dry benzene (100 ml) in the presence of phosphorus oxychloride (8.3 ml) for 30 hours at 65°-70° C. gave an oil which was purified by column chromotography on a neutral alumina column (100 g) eluted with hexane to give as an oil. A solution of this base (2.5 g) in methanol (10 ml) was treated with 57% hydroiodic acid (1.3 ml) to give 2-(2-morpholinophenyl)-1,1,3,3-tetramethylguanidine hydroiodide as a pale yellow crystalline solid (m.p. 215°-216° C.) which was recrystallised from a 2:3 mixture of methanol and ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05373008 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-64c6eecc85e74619b05e57d1fddc6a76 |
| Source note | uspto-grants-1994_12 |