HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → Methyl Isocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | 2,2-Diethoxyethylamine | HCID 69524 | — |
| Reactant | 1,3-Dihydro-1-methyl-3-(2-propyn-1-yl)-2H-imidazol-2-one | HCID 15065505 | — |
| Product | Methyl Isocyanate | HCID 12228 | — |
| Product | HCID 19753286 | HCID 19753286 | — |
Reaction Steps
The 1,3-dihydro-1-(2-propynyl)-2H-imidazol-2-one intermediates were prepared as outlined in Scheme 2 for the synthesis of 1,3-dihydro-1-methyl-3-(2-propynyl)-2H-imidazol-2-one (X). Aminoacetaldehyde diethyl acetal was reacted with propargylbromide to give a mixture of the tertiary and secondary amines VII and VIII which were separated by chromatography on silica gel. Treatment of VIII with methyl isocyanate gave IX and this was heated in aqueous oxalic acid to give 1-methyl-3-(2-propynyl)-2H-imidazol-2-one (X).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05157124 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-086015f787cf4bb298d0ead5fb4c3436 |
| Source note | uspto-grants-1992_10 |