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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505907Generated: October 30, 2026

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

https://huagongshe.com/reaction/1505907

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 numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-860115fc99df451d9dbf2ddc01d96622
Source noteuspto-grants-2015_12