HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237017Generated: October 28, 2026
1-(4-Fluorophenyl)-4-[(4-nitrophenyl)sulfonyl]piperazine → HCID 21314924, compound
https://huagongshe.com/reaction/237017
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(4-Fluorophenyl)-4-[(4-nitrophenyl)sulfonyl]piperazine | HCID 1068502 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21314924 | HCID 21314924 | 47.1% |
Reaction Steps
A mixture of 5.00 g (0.0137 m) of 1-[(p-nitrophenyl)sulfonyl]-4-(p-fluorophenyl)piperazine, 0.2 g of platinum oxide, and 150 ml of chloroform is shaken under hydrogen on a Parr hydrogenation apparatus for one hour. The mixture is then filtered through a sintered glass funnel containing activated carbon and sand to remove the catalyst. The filtrate is concentrated in vacuo and then extracted with methylene chloride/aqueous sodium bicarbonate. The organic layer is filtered through anhydrous sodium sulfate and taken to dryness. The residue is crystallized from methanol to give 2.16 g of 1-[(p-aminophenyl)sulfonyl]-4-(p-fluorophenyl)piperazine containing a minor impurity. Recrystallization from methanol gives an analytical sample with a melting point of 180.5°-181.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04159331 |
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| Source dataset | uspto-grants-1979_06 |
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| ORD ID | ord-c0dabf1b92554995b61bf588bccbc459 |
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| Source note | uspto-grants-1979_06 |
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