HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087814Generated: October 25, 2026
Benzene → N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamide
https://huagongshe.com/reaction/1087814
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(4-Benzylpiperazin-1-yl)aniline | HCID 737259 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamide | HCID 960610 | 99% |
Reaction Steps
To a solution of 8.5 g (0.03 mole) of the base of 4-[4-(phenylmethyl)-1-piperazinyl)benzeneamine and 16.0 g (0.16 mole) of triethylamine in 450 ml of ethyl acetate was added, dropwise, a solution of 2.5 g (0.035 mole) of acetyl chloride in 50 ml of ethyl acetate. The mixture was magnetically stirred for 3 hr and then heated at reflux for 1 hr. The excess acetyl chloride was co-distilled with benzene and the resulting oil was shaken in 400 ml of 10% sodium hydroxide solution. The suspended tan solid was collected by filtration, washed thrice with 100 ml portions of water, and air dried to give 9.7 g (99%) of crude product. A one gram portion was recrystallized from benzene/petroleum ether to give 100 ml of cream colored solid, m.p. 159°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04960776 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-dc396a8e47794e67bb832c3e3f9b2130 |
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| Source note | uspto-grants-1990_10 |
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