HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076787Generated: November 3, 2026
Dimethyl Sulfoxide → HCID 21537802, compound
https://huagongshe.com/reaction/1076787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Calcium Carbonate | HCID 10112 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | 1,1'-(3-Chloropropane-1,1-diyl)dibenzene | HCID 190135 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | (+-)-2-Butanol | HCID 6568 | — |
| Product | HCID 21537802 | HCID 21537802 | 81.2% |
Reaction Steps
N-benzylpiperazine in the amount of 1.76 g (0.01 mole), 2.3 g (0.01 mole) of 3,3-diphenylpropyl chloride, 1.5 g (0.015 mole) of calcium carbonate, and 2 ml of dimethyl sulfoxide were mixed with 20 ml of secondary butanol, and the resulting solution was heated at the refluxing temperature for 2.5 hours. The reaction liquid was filtered after being left to cool, and the filtrate was concentrated under reduced pressure to produce an oily residue, which was shaken with ether and water, and the ether layer dried. Then, dry hydrogen chloride gas was passed through the ether solution while cooling the solution to precipitate 1 -(3,3-diphenylpropyl)-4-benzylpiperazine dihydrochloride, whose crystals were recrystallized from methanol to obtaine 3.6 g (81.2% yield) of pure crystals with a melting point of 187° -188°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03957790 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-78b92797a10140acb6866b7b2fe4b2f3 |
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| Source note | uspto-grants-1976_05 |
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