HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659630Generated: October 31, 2026
Acetic Acid → 1-(4-Bromophenyl)-2-cyclohexylidenehydrazine
https://huagongshe.com/reaction/659630
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Bromophenylhydrazine hydrochloride | HCID 12157 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Bromophenyl)-2-cyclohexylidenehydrazine | HCID 4167253 | 92% |
Reaction Steps
A 250-mL round-bottomed flask was charged with 1-(4-bromophenyl)hydrazine hydrochloride (10 g, 45.05 mmol, 1.00 equiv) in EtOH (120 mL). To this was added cyclohexanone (8.8 g, 89.80 mmol, 2.00 equiv) and acetic acid (2.7 g, 45.00 mmol, 1.00 equiv). The resulting mixture was heated to 105° C. in an oil bath for about 1 hour. The reaction progress was monitored by TLC (EtOAc:PE=1:1). Upon completion, the reaction mixture was cooled down to room temperature and filtered off to obtain 1-(4-bromophenyl)-2-cyclohexylidenehydrazine as a yellow solid (11 g, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08080566B1 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-0070776a323643a1aaff854f6b68ae38 |
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| Source note | uspto-grants-2011_12 |
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