HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carbonyl chloride → 3-(5-Nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carbonyl chloride | HCID 20325933 | — |
| Reactant | 3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carboxylic acid | HCID 20325964 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(5-Nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid anhydride | HCID 54363990 | — |
Reaction Steps
Add a solution of 0.64 g of 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid chloride dropwise to a warm solution of 0.60 g of 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid in 10 ml of dioxane and 0.48 ml of pyridine at 40° C. Stir the resulting reaction mixture at from 45° to 50° C for 6 hours. Draw off the formed precipitate and recrystallize it from dimethylformamide to obtain 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxylic acid anhydride [m.p. 262° to 264° C].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04093812 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-6cabb35fbf964e4ebfb6a7393a19d1a9 |
| Source note | uspto-grants-1978_06 |