Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 23508484 | HCID 23508484 | 46% |
Reaction Steps
1.08 g of phenylhydrazine was dissolved in 10 ml of pyridine, and 0.78 g of acetic anhydride was added thereto under cooling with ice, followed by stirring for 20 minutes. Then, 2.0 g of 4-methoxybenzoyl chloride was added thereto, followed by stirring at room temperature for 15 hours. After water was added to the reaction mixture, the product was extracted with ethyl acetate. The organic layer was washed with 5% hydrochloric acid and a 5% aqueous solution of sodium hydroxide, and dried over anhydrous sodium sulfate. After the solvent was distilled off, the resulting crude product was purified by silica gel column chromatography (using a 40:1 mixture of chloroform and methanol as the eluent) to obtain 1.0 g of N′-acetyl-4-methoxy-N-phenylbenzohydrazide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06762205B1 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-8783f07cbaeb409a90167cdce6bb584f |
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| Source note | uspto-grants-2004_07 |
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