HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Ethoxy-4-nitrobenzohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 3-Ethoxy-4-nitrobenzoic acid | HCID 22397509 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Ethoxy-4-nitrobenzohydrazide | HCID 89995586 | 95% |
Reaction Steps
3-Ethoxy-4-nitrobenzoic acid (PCT Int Appl. 2008003958, 1.06 g 5.02 mmole) was stirred with dry THF (10 mL) and triethylamine (0.86 mL, 6.1 mmol) and the solution was cooled in an ice bath. Ethyl chloroformate (0.56 mL, 5.85 mmol) was added dropwise and the reaction was stirred in the ice bath for 15 minutes. Hydrazine hydrate (1.27 mL, 26 mmol) was added in one portion and the reaction stirred in the ice bath for 5 minutes and then at 20° C. for 1 hour. The reaction was concentrated in vacuo, partitioned between EtOAc (100 mL) and saturated aqueous sodium bicarbonate (15 mL). The organic layer was collected, washed with brine, dried over sodium sulfate and concentrated in vacuo to afford the title compound (1.07 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09334286B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-a4140a088ac8450b99941c6cdce08882 |
| Source note | uspto-grants-2016_05 |