HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,3,6-Tetrahydrophthalimide → N-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-1,2,3,6-tetrahydrophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,3,6-Tetrahydrophthalimide | HCID 6808 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | 1-(2-Hydroxyethyl)-2-methyl-5-nitroimidazole tosylate | HCID 86734258 | — |
| Product | N-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-1,2,3,6-tetrahydrophthalimide | HCID 21491658 | — |
Reaction Steps
1,2,3,6-Tetrahydrophthalimide is converted to the potassium salt and reacted with 1-(2-hydroxyethyl)-2-methyl-5-nitroimidazole tosylate according to the procedure described in Example 13. The crude reaction mixture obtained is concentrated and the concentrate distributed between water and toluene. The toluene layer is separated and the solvent is evaporated to leave a residue which is recrystallized from 2-propanol, affording N-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-1,2,3,6-tetrahydrophthalimide melting at about 118°-123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03997572 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-90b718b0ea0140c8a9bcde1fb2cba8b1 |
| Source note | uspto-grants-1976_12 |