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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888435Generated: November 1, 2026

Piperidine → 1-(3-Bromo-5-methoxybenzyl)piperidine

https://huagongshe.com/reaction/1888435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Bromo-5-methoxybenzaldehydeHCID 10608698—
SolventDichloromethaneHCID 6344—
Product1-(3-Bromo-5-methoxybenzyl)piperidineHCID 5826657169%

Reaction Steps

To a pre-stirred solution of 3-bromo-5-methoxybenzaldehyde (0.56 g, 2.61 mmol) and piperidine (0.29 mL, 3.93 mmol) in DCM (10 mL) at 0° C. was added sodium borohydride (197 mg, 5.22 mmol) in portions. The reaction mixture was allowed to warm to ambient temperature and stirred for an additional 2 h. The reaction was quenched by the addition of water (30 mL) and extracted into ethyl acetate (75 mL) then washed with water (50 mL) then the organic phase was dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to afford the title compound as a colourless oil (510 mg, 69%) that was used in the next step without further purification. 1H NMR (CDCl3, 400 MHz): 7.08-7.06 (m, 1H), 6.94-6.91 (m, 1H), 6.83-6.80 (s, 1H), 3.79 (s, 3H), 3.39 (s, 2H), 2.40-2.30 (s, 4H), 1.61-1.51 (m, 4H), 1.47-1.38 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-68c4936ffead43dbbc91c291c5dee62b
Source noteuspto-grants-2013_08