Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-[(2-Fluorophenyl)methyl]-1H-pyrrole-2-carbaldehyde | HCID 1089184 | — |
| Product | HCID 57489126 | HCID 57489126 | — |
Reaction Steps
The Grignard reagent of 4-phenylpiperaznopropylmagnesium bromide is added to benzane and the mixture is refluxed at 45°C for 1 hour. The mixture is permitted to cool and a solution of 1-(2-fluorobenzyl)pyrrole-2-carboxaldehyde in ether is added and then the mixture is stirred at 45°C for 20 hours. The reaction is permitted to cool, poured into ammonium chloride solution and the ammonium chloride solution is stirred for 30 minutes and extracted with chloroform. The combined chloroform extracts are washed well with water, dried and filtered and the solvent removed leaving 1-[1-(2-fluorobenyl)-2-pyrryl]-4-(4-phenylpiperazino)butanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04053599 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-53d15405665a4fc39bf26f8452d6f27f |
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| Source note | uspto-grants-1977_10 |
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