HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycidol → HCID 14638280, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycidol | HCID 11164 | — |
| Reactant | HCID 14638217 | HCID 14638217 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 14638280 | HCID 14638280 | 83% |
Reaction Steps
A suspension containing 0.96 g of 4-(4-ethoxycarbonyl-1-piperazinyl)-2-methyl-6,7-dihydro-8H-pyrimido[5,4-b][1,4]oxazin-7-one (Example 1), 0.44 g of 2,3-epoxy-1-propanol, 0.0966 g of tetra(n-butyl)-ammonium bromide and 20 ml of abs. benzene is boiled under stirring for 5 hours and left to stand at room temperature overnight. The crystals are filtered, washed with diisopropyl ethyl and dried to give 0.98 g (83%) of the product, m.p.: 146°-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04748175 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-d74556d18e024ee88bef5af18ecdb376 |
| Source note | uspto-grants-1988_05 |