HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004950Generated: October 30, 2026
1-Benzyl-4-piperidone → 4-(2H-1,3-Benzodioxol-5-yl)-1-benzylpiperidin-4-ol
https://huagongshe.com/reaction/1004950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Bromo-3,4-(methylenedioxy)benzene | HCID 75831 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2H-1,3-Benzodioxol-5-yl)-1-benzylpiperidin-4-ol | HCID 22128034 | — |
Reaction Steps
To 1.46 g of magnesium shavings, which had previously been covered with tetrahydrofuran, was added dropwise a solution of 12.06 g (60 mmol) of 5-bromo-benzo[1,3]dioxol in 30 ml of absolute tetrahydrofuran, followed by 11.35 g (60 mmol) of 1-benzyl-4-piperidone. The reaction mixture was stirred at 50° C. for 1 hour, then poured on to ice and ammonium chloride solution. The 4-benzo[1,3]dioxol-5-yl-1-benzyl-piperidin-4-ol formed was extracted with ethyl acetate and crystallized upon concentration of the solution. There were obtained 10.85 g (58% of theory) of white crystals; m.p.: 144° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06051712 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-481309fe81474a30be03ed5589a8b2b5 |
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| Source note | uspto-grants-2000_04 |
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