HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639070Generated: October 26, 2026
1-Butanol → 4-(Piperazin-1-yl)benzonitrile hydrochloride
https://huagongshe.com/reaction/1639070
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzonitrile, 4-bromo- | HCID 12162 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(Piperazin-1-yl)benzonitrile hydrochloride | HCID 2733994 | — |
Reaction Steps
A mixture of 27.3 g (0.15 mole) of p-bromobenzonitrile, 38.7 g (0.45 mole) of piperazine and 42.0 g (0.30 mole) of solid potassium carbonate in a total volume of 60 ml of n-butanol was heated at reflux for 16 hr under a nitrogen atmosphere. The mixture was concentrated under reduced pressure and the slurry partitioned between 10% sodium hydroxide and chloroform. The chloroform layer was separated, dried over magnesium sulfate and concentrated under reduced pressure to give an oil. The oil was eluted through a 400 g silica gel column with a 10% methanol in methylene chloride mixture. The appropriate fractions were concentrated under reduced pressure to give a golden oil. Trituration of this oil with ethyl acetate gave a white powder. The collected white powder was stirred for 15 min in ethereal hydrogen chloride and recrystallized from methanol-water to give 1.5 g (4.5%)* of white solid, m.p. 160° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04882330 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-f32a01d80fc047809de585231398b386 |
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| Source note | uspto-grants-1989_11 |
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