HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetohydrazide → HCID 67036847, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetohydrazide | HCID 14039 | — |
| Reactant | 3,4-Dimethoxy-5-nitrobenzoic acid | HCID 21928624 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67036847 | HCID 67036847 | — |
Reaction Steps
To a stirred solution of 3,4-dimethoxy-5-nitrobenzoic acid (0.438 g, 1.93 mmol) in tetrahydrofuran (10 mL) at room temperature was added 1,1-carbonyldiimidazole (0.343 g, 2.12 mmol) in one portion and the mixture was stirred at room temperature for one hour, then at 70° C. for two hours, whereupon acetic hydrazide (0.157 g, 2.12 mmol) was added. The resulting was stirred at room temperature for thirty minutes, then at 70° C. for two hours. After cooling to room temperature, the mixture was poured onto ice-water (100 mL) and the precipitate was filtered off and washed with water. 3,4-Dimethoxy-5-nitro-benzoic acid N′-acetyl-hydrazide was obtained as a white solid (0.296 g, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08907099B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-2af4c2df838148c385a279533ce451af |
| Source note | uspto-grants-2014_12 |