HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797833Generated: October 26, 2026
Benzoyl chloride → 1-Benzoyl-2-(4-iodobenzoyl)hydrazine
https://huagongshe.com/reaction/1797833
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 4-Iodobenzenecarbohydrazide | HCID 306104 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Benzoyl-2-(4-iodobenzoyl)hydrazine | HCID 4808937 | 97% |
Reaction Steps
Into a 300 mL three-neck flask was put 15 g (57 mmol) of 4-iodobenzoylhydrazine, 15 mL of N-methyl-2-pyrrolidone (NMP) was added thereto, and the mixture was stirred for 10 minutes at a room temperature. After the stirring, 50 mL of a mixed solution of 5 mL of N-methyl-2-pyrrolidone and 7.9 mL (69 mmol) of benzoyl chloride was dripped into the solution through a dropping funnel, and the solution was stirred at a room temperature for 18 hours. After the stirring, water was added into the solution, and a solid was precipitated. The precipitated solid was collected by suction filtration. The collected solid was added into about 500 mL of a saturated aqueous solution of sodium hydrogen carbonate, stirred, and washed. After the washing, the mixture was subjected to suction filtration to obtain a solid. The obtained solid was added into about 500 mL of water, stirred, and washed. After the washing, the mixture was subjected to suction filtration to obtain a solid. The obtained solid was washed with methanol to give 20 g of a powdery white solid in a yield of 97%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08343639B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-f0ece7b2d05d4470964092363d930256 |
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| Source note | uspto-grants-2013_01 |
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