Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 11-Bromoundecanoic acid | HCID 17812 | — |
| Reactant | 1-Piperazinecarboxaldehyde | HCID 82191 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53950422 | HCID 53950422 | 70% |
Reaction Steps
26.5 g (0.1 mole) quantity of 11-bromoundecanoic acid was dissolved in 300 ml of methanol, and 5 to 6 drops of sulfuric acid was added thereto and the mixture was stirred at room temperature for 24 hours and concentrated. 500 ml quantity of ethyl acetate was added to the residue and the solution was washed sequentially with 100 ml of water and 100 ml of a brine, and then dried over anhydrous magnesium sulfate. Ethyl acetate was evaporated under reduced pressure and the residue was dissolved in 200 ml of dimethylformamide. To the solution were added 11.4 g (0.1 mole) of formylpiperazine and 18.5 g (0.22 mole) of sodium hydrogencarbonate. The mixture was stirred at 80 ° C for 3 hours and concentrated under reduced pressure. 500 ml quantity of ethyl acetate was added to the residue and the mixture was washed sequentially with 100 ml of water and 100 ml of a brine, and then dried over anhydrous magnesium sulfate. Ethyl acetate was evaporated under reduced pressure. To the residue were added 300 ml of methanol and 50 ml of concentrated hydrochloric acid, and the mixture was refluxed for 3 hours. The solvent was evaporated under reduced pressure and the precipitated white crystals were washed with acetone, giving 25 g (yield: 70 %) of 11-(1-piperazinyl)undecanoic acid methyl ester as a hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05318970 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-8669b1b4f6ad467ba4c3b1a6f7f1f5ce |
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| Source note | uspto-grants-1994_06 |
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