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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Bromo-5-methoxybenzaldehyde | HCID 10608698 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3-Bromo-5-methoxybenzyl)piperidine | HCID 58266571 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216980B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-126c368ee5964b87a7c8fdb8caf5259c |
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| Source note | uspto-grants-2015_12 |
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