HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619101Generated: November 1, 2026
Triethylamine → Cyclobutanecarboxylic acid, 2-(3-bromophenyl)hydrazide
https://huagongshe.com/reaction/1619101
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromophenylhydrazine hydrochloride | HCID 33757 | — |
| Reactant | Cyclobutanecarbonyl chloride | HCID 78705 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Cyclobutanecarboxylic acid, 2-(3-bromophenyl)hydrazide | HCID 67269294 | 60% |
Reaction Steps
Triethylamine (6.90 mL, 49.22 mmol) was added dropwise to a suspension of 3-bromophenylhydrazine hydrochloride (5.00 g, 22.37 mmol) in dichloromethane (60 mL) to give a solution. The mixture was cooled in an ice-salt bath and then cyclobutanecarbonyl chloride (2.68 mL, 23.49 mmol) in dichloromethane (10 mL) was added dropwise at such a rate that the internal temperature did not exceed −10° C. After the addition, the mixture was stirred at −5° C. to −10° C. for 1.5 hours. The cooling bath was removed and the mixture was stirred for a further 2 hours at room temperature. The mixture was evaporated in vacuo and 4% aqueous sodium hydrogen carbonate solution was added. The mixture was filtered and the semi-solid was washed with 4% aqueous sodium hydrogen carbonate solution, water and diethyl ether and dried in vacuo to give the title compound (3.60 g, 60%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772288B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-342f36b22df941aab92e27b2fddea60e |
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| Source note | uspto-grants-2014_07 |
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