HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → N'-benzoyl-4-bromobenzohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 4-Bromobenzohydrazide | HCID 22219 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N'-benzoyl-4-bromobenzohydrazide | HCID 3789270 | 80% |
Reaction Steps
Subsequently, 2.0 g (13.9 mmol) of the 4-bromobenzohydrazide obtained in (i) above was put in a 300-mL three-neck flask, 7 mL of N-methyl-2-pyrrolidone (abbreviation: NMP) was added thereto, and the mixture was stirred. Thereafter, a mixture of 2.5 mL of N-methyl-2-pyrrolidone and 2.5 mL (21.5 mmol) of benzoyl chloride was dripped through a 50-mL dropping funnel, and the mixture was stirred at 80° C. for 3 hours. The obtained solid was washed with water and a sodium carbonate aqueous solution in this order and collected by suction filtration. Then, the solid was recrystallized with acetone; thus, 3.6 g of a white solid of 1-benzoyl-2-(4-bromobenzoyl)hydrazine that was an object was obtained in the yield of 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09112170B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-316e863fba134d848788ff7fb569cca5 |
| Source note | uspto-grants-2015_08 |