HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → HCID 20566541, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 11378721 | HCID 11378721 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Butyl ether | HCID 8909 | — |
| Product | HCID 11378721 | HCID 11378721 | — |
| Product | HCID 20566541 | HCID 20566541 | 20% |
Reaction Steps
A solution of diazomethane in ether(prepared from 200 g of N-nitrosomethylurea) is introduced in portions over the course of 3 days into a solution of 25.0 g (0.15 mol) of 1,3-diacetyl-4-imidazolin-2-one and 5.0 g of copper-I chloride in 250 ml of di-n-butyl ether at 80°-90°. The solution is then filtered, the residue is repeatedly eluted with benzene and the combined filtrates are concentrated in vacuo. Chromatography of the crude product on silica gel gives 10.3 g of unconverted 1,3-diacetyl-4-imidazolin-2-one and 3.6 g (about 20%) of 2,4-diacetyl-2,4-diaza-bicyclo[3,1,0]hexan-3-one as colourless crystals of melting point 134°-136° C. (from ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04294973 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-c464c74e4e494fda83604d052727b36b |
| Source note | uspto-grants-1981_10 |