Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Reactant | Homopiperazine dihydrochloride | HCID 23441047 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Benzyl-1,4-diazepane | HCID 228365 | — |
Reaction Steps
A mixture of 101 mg of homopiperazine, 175 mg of homopiperazine dihydrochloride, 3 mL of ethanol was heated to 70° C. into a solution. 0.115 mL of benzyl chloride was added and the mixture was stirred at 70° C. for 3 hours. After cooling to room temperature, ethanol was removed under reduced pressure, and 20 mL of aqueous 2N sodium hydroxide solution was added to the solution, which was extracted with 20 mL×2 of ethyl acetate. The organic layers were combined, washed with 20 mL of saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated to give 1-benzyihomopiperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06686353B1 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-96396319e79d43c4b618c653f72517a8 |
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| Source note | uspto-grants-2004_02 |
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