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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291132Generated: October 31, 2026

4-Bromobenzyl bromide → HCID 677772, compound

https://huagongshe.com/reaction/1291132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzyl bromideHCID 68527—
ReactantPiperidin-4-olHCID 79341—
SolventDimethylformamideHCID 6228—
ProductHCID 677772HCID 677772100%

Reaction Steps

0.202 g (0.002 mol) of 4-hydroxypiperidine and 0.55 g (0.0022 mol) of 4-bromobenzyl bromide were dissolved in 5 ml of dimethylformamide and stirred at room temperature for 2 hrs. The solvent was distilled off and the residue was taken up in dichloromethane and washed with sat. bicarbonate solution and sodium chloride solution. The organic phase was dried over sodium sulfate and concentrated. 0.54 g (100%) of 1-(4-bromo-benzyl)-piperidin-4-ol was obtained as a colorless oil. MS: me/e (% basic peak)=271, 269 (C12H16BrNO30 , 73, 76), 270, 268 (79, 70), 171, 169 (99, 100), 114 (64), 100 (60).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-b0cce427147d4cf58f2bbf443e200515
Source noteuspto-grants-1998_05