Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 4-(4-bromophenyl)-4-methylpiperidine-1-carboxylateHCID 57489651—
SolventEthanolHCID 702—
Product4-(4-Bromophenyl)-4-methylpiperidineHCID 63156611—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382246B2
Source datasetuspto-grants-2016_07
ORD IDord-8f7f1d4951ec4910aadeae15e8fbccbd
Source noteuspto-grants-2016_07