Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383594Generated: November 1, 2026

Methyl iodide → 4-(4-Bromophenyl)-1-methylpiperidin-4-ol

https://huagongshe.com/reaction/2383594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Bromophenyl)-4-hydroxypiperidineHCID 93911—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-(4-Bromophenyl)-1-methylpiperidin-4-olHCID 1065963494.1%

Reaction Steps

A reaction mixture of 4-(4-bromophenyl)piperidin-4-ol (1.5 g, 5.9 mmol), methyl iodide (0.4 mL, 6.4 mmol), and K2CO3 (1.2 g, 8.8 mmol) in acetone was stirred at rt for 90 min The reaction was diluted with EtOAc and water was added. The resulting mixture was extracted with EtOAc and the combined organic extracts were dried over MgSO4 and concentrated to give the title compound as a yellow solid (1.5 g, used without further purification). 1H NMR (400 MHz, CDCl3) δ 7.40 (d, J=8.1 Hz, 2H), 7.29 (d, J=8.1 Hz, 2H), 3.20 (br s, 1H), 2.64-2.61 (m, 2H), 2.39 (t, J=11.8 Hz, 2H), 2.21 (s, 3H), 2.03-1.96 (m, 2H), 1.64-1.61 (m, 2H); MS ESI 270.0 [M+H]+, calcd for [C12H16BrNO+H]+ 270.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263596B2
Source datasetuspto-grants-2012_09
ORD IDord-156ef4a75713462f9e8909fd495e6e90
Source noteuspto-grants-2012_09