HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-(4-Methoxybenzoyl)-2-(4-methoxyphenyl)hydrazinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | 2-(4-Methoxyphenyl)hydrazinecarboxamide | HCID 341971 | — |
| Reactant | Tetrahydrofuran ethyl acetate | HCID 21939870 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4-Methoxybenzoyl)-2-(4-methoxyphenyl)hydrazinecarboxamide | HCID 22341581 | 61.9% |
Reaction Steps
To a suspension of 2-(4-methoxyphenyl)hydrazinecarboxamide (1.81 g, 9.99 mmol) in 20 mL of toluene, pyridine (1.01 mL, 12.5 mmol) and then a solution of 4-methoxybenzoyl chloride (2.13 g, 12.5 mmol) in 10 mL of toluene were added. The mixture was refluxed with stirring for 1 hour. After cooling, 500 mL of ethyl acetate-tetrahydrofuran (9:1) and 100 mL of water were added to the mixture. After vigorous shaking, an insoluble material was isolated by filtration and dired in vacuo to give 2-(4-methoxybenzoyl)-2-(4-methoxyphenyl)hydrazinecarboxamide (1.95 g, 61.9% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06927230B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-edbe269e48cb4d83b9b53cf0ecce9ca8 |
| Source note | uspto-grants-2005_08 |