HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 178481284, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | N,N-Dimethylurea | HCID 11737 | — |
| Reactant | HCID 178511715 | HCID 178511715 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178481284 | HCID 178481284 | 75% |
Reaction Steps
To a mixture of trans-4-aminocyclohexanol (5.00 g, 43.4 mmol), N,N-dimethylurea (3.82 g, 43.4 mmol), 37% formalin (50 ml), N-methylmorpholine (9.54 ml, 86.8 mmol) and dioxane (10 ml) was added toluene (200 ml), and the mixture was heated for about 5 hours while removing water for azeotropic distillation. Low boiling matters were distilled away from the reaction mixture under reduced pressure, and the residue was purified by silica gel column chromatography (methylene chloride/methanol=50/1-10/1) to give 7.40 g of trans-5-(4-hydroxycyclohexyl)-1,3-dimethylhexahydro-2-oxo-1,3,5-triazine as colorless solid (75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753670 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-6c42842c47cc4db78bd37a9ead13f8bc |
| Source note | uspto-grants-1998_05 |