HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 1-Methyl-4-nitro-1H-imidazole-2-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-Methyl-4-nitro-1H-imidazole-2-carboxylic acid | HCID 12067998 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Methyl-4-nitro-1H-imidazole-2-carbonyl chloride | HCID 19108629 | — |
Reaction Steps
To a suspension of 1-methyl-4-nitroimidazole-2-carboxylic acid (3.00 g, 17.5 mmol) in dry THF (30 mL) was slowly added oxalyl chloride (12 mL). The reaction mixture was heated to reflux under a drying tube for 45 minutes at which time the excess oxalyl chloride and THF were removed under reduced pressure and the acid chloride coevaporated twice with dry CH2Cl2 (20 mL each) yielding 1-methyl-4-nitroimidazole-2-carbonyl chloride as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05273991 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-c4c400ae5f8048268425aac0e1979e00 |
| Source note | uspto-grants-1993_12 |