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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505898Generated: October 31, 2026

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

https://huagongshe.com/reaction/1505898

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 numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-126c368ee5964b87a7c8fdb8caf5259c
Source noteuspto-grants-2015_12