HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986166Generated: October 28, 2026
Phenylhydrazine hydrochloride → HCID 86741574, compound
https://huagongshe.com/reaction/986166
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylhydrazine hydrochloride | HCID 60962 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 14032496 | HCID 14032496 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 86741574 | HCID 86741574 | 93% |
Reaction Steps
A mixture of 1-acetyl-4-(4-bromo-2-fluorobenzoyl)piperidine (16.6 g, 0.051 mol), phenylhydrazine hydrochloride (16.6 g, 0.11 mol), sodium acetate, (22.2 g) and isopropanol (250 ml) was stirred and refluxed for 4 hours. The reaction stood at ambient temperature for 16 hours, and then was filtered. The filtercake was treated with water, and the insoluble hydrazone was collected and dried to yield 13.7 g. The isopropanol filtrate was concentrated in vacuo to a solid, which when triturated with ether yielded 6.1 g more of the hydrazone (total yield 19.8 g; 93%). The phenylhydrazone was a mixture of the two geometric isomers. A 3.5 g sample of the compound was recrystallized from isopropanol to yield 2.1 g of the phenylhydrazone; mp 174°-176° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04710573 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-ec9f587f5ed54691a546e5057011201e |
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| Source note | uspto-grants-1987_12 |
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