HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505865Generated: October 30, 2026
Formaldehyde → 4-(4-Bromobenzyl)-1-methylpiperidine
https://huagongshe.com/reaction/1505865
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 20689421 | HCID 20689421 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 4-(4-Bromobenzyl)-1-methylpiperidine | HCID 58266845 | 98.1% |
Reaction Steps
A mixture of 4-(4-bromobenzyl)-piperidine (290 mg, 1.14 mmol), formic acid (12 mL) and 37% aqueous formaldehyde (0.30 mL, 3.75 mmol) was divided into three portions. Each portion was heated at 150° C. for 5 minutes in a microwave reactor. The combined cold mixture was loaded onto a 5 g SCX-2 cartridge which was then washed with methanol (30 mL) then 2 N ammonia in methanol (50 mL). Concentration of the combined basic fractions in vacuo gave the title compound (300 mg, 98%) as a colourless oil. LCMS (Method B): RT=2.18 min, M+H+=268, 270.
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-7ee188f646ee48cbb00f0d5717a3ed76 |
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| Source note | uspto-grants-2015_12 |
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