HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050544Generated: November 1, 2026
Potassium Hydroxide → 4-(4-Bromophenyl)-4-methylpiperidine
https://huagongshe.com/reaction/1050544
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 4-(4-bromophenyl)-4-methylpiperidine-1-carboxylate | HCID 57489651 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(4-Bromophenyl)-4-methylpiperidine | HCID 63156611 | — |
Reaction Steps
To a solution of ethyl 4-(4-bromophenyl)-4-methylpiperidine-1-carboxylate (284) (5.36 g, 16 mmol) in EtOH (75 mL) was added KOH (17.9 g, 320 mmol). The resulting mixture was stirred at 80° C. for overnight before being cooled down to RT. The solvent was removed and the residue was partitioned in water (30 mL) and DCM (20 mL). The layers were separated and the aqueous layer was extracted with DCM (10 mL×5). The combined organic layers were washed with brine, dried, and concentrated in vacuo to give crude 4-(4-bromophenyl)-4-methylpiperidine (285) in quantitative yield, which was used directly in next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382246B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-8f7f1d4951ec4910aadeae15e8fbccbd |
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| Source note | uspto-grants-2016_07 |
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