Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888444Generated: November 4, 2026

Triethylamine → 1-(4-Bromobenzyl)-3-methyl-piperidin-3-ol

https://huagongshe.com/reaction/1888444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Bromobenzyl bromideHCID 68527—
Reactant3-Methylpiperidin-3-olHCID 22496626—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Bromobenzyl)-3-methyl-piperidin-3-olHCID 5826659088%

Reaction Steps

A mixture of 4-bromobenzyl bromide (0.50 g, 2.0 mmol), triethylamine (0.42 mL, 3.0 mmol) and 3-methyl-piperidin-3-ol (0.46 g, 4.0 mmol) in THF (20 mL) was stirred at ambient temperature for 16 h. The reaction mixture was evaporated and the resultant residue diluted with saturated aqueous sodium bicarbonate solution and extracted with ethyl acetate (2×50 mL). The combined organic layer was dried over sodium sulfate, filtered and evaporated to afford the title compound (0.50 g, 88%). 1H NMR (CDCl3, 300 MHz): 7.49-7.43 (m, 2H), 7.23-7.15 (m, 2H), 3.78 (s, 2H), 3.69-3.59 (m, 2H), 2.63-2.51 (m, 2H), 2.14 (br s, 1H), 1.77-1.49 (m, 4H), 1.15 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-6c8021d9828344afaf7f637f5e9fd437
Source noteuspto-grants-2013_08