HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076734Generated: October 31, 2026
Benzoyl chloride → N'-benzoyl-4-bromobenzohydrazide
https://huagongshe.com/reaction/2076734
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 4-Bromobenzohydrazide | HCID 22219 | — |
| Solvent | Water | HCID 962 | — |
| Product | N'-benzoyl-4-bromobenzohydrazide | HCID 3789270 | — |
Reaction Steps
In a 200 mL three-necked flask were placed 15 g (71 mmol) of 4-bromobenzoylhydrazine and 20 mL of N-methyl-2-pyrrolidone (abbreviation: NMP). To this mixture was dripped a solution of 9.4 mL (81 mmol) of benzoyl chloride in 5 mL solution of N-methyl-2-pyrrolidone through a 50 mL dropping funnel. This solution was stirred at 80° C. for 3 hours under a stream of nitrogen. After a predetermined time, this solution was added to about 100 mL of water, and the precipitated solid was collected by suction filtration. The collected solid was washed with methanol, and 19 g of a white powder, which was a target substance, was obtained at a yield of 84%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07927720B2 |
|---|
| Source dataset | uspto-grants-2011_04 |
|---|
| ORD ID | ord-d983f28795d04a6ea9460862e3a49a02 |
|---|
| Source note | uspto-grants-2011_04 |
|---|