Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-(3-Methoxybenzyl)-2,5-piperazinedione | HCID 22342919 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 218594-59-3 | HCID 22342893 | 85.9% |
Reaction Steps
To a 100-mL round-bottomed flask was added 3-(3-methoxybenzyl)-2,5-piperazinedione (201 mg, 0.858 mmol), 5 mL of THF and BH3.DMS (0.326 mL, 3.43 mmol, Aldrich, St. Louis, Mo.). The reaction mixture was stirred at 70° C. for 18 h and then diluted with 1N NaOH (12 mL) and extracted with CH2Cl2 (2×50 mL). The organic extracts were washed with saturated aqueous NaCl (5 mL) and dried over Na2SO4. The solution was filtered and concentrated in vacuo to give the crude 2-(3-methoxybenzyl)piperazine (152 mg) as a colorless tar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431563B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-3abeda7c35f6410a9d1347564d2e1778 |
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| Source note | uspto-grants-2013_04 |
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