HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119349Generated: November 2, 2026
Sodium Iodide → 1-[4-(Methylsulfonyl)benzyl]homopiperazine
https://huagongshe.com/reaction/2119349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Reactant | 4-(Methylsulfonyl)benzyl Bromide | HCID 2733581 | — |
| Reactant | Homopiperazine dihydrochloride | HCID 23441047 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[4-(Methylsulfonyl)benzyl]homopiperazine | HCID 23441023 | 65.4% |
Reaction Steps
A mixture of 120 mg of homopiperazine, 216 mg of homopiperazine dihydrochloride salt, 3 mL of ethanol was heated to 70° C. into a solution. To this solution were added sequentially 383 mg of sodium iodide and 250 mg of 4-(methylsulfonyl)benzyl bromide, followed by stirring at 70° C. for 14 hours. After the solution was cooled to room temperature, ethanol was removed under reduced pressure and 20 mL of aqueous 2N sodium hydroxide was added and the mixture was extracted with 20 mL×2 of ethyl acetate. The organic layers were combined, washed with 20 mL of aqueous saturated sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated to give 176 mg of 1-[4-(methylsulfonyl)benzyl]homopiperazine.
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-de6286b21d5943d5a28510eaf4308cce |
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| Source note | uspto-grants-2004_02 |
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