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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888402Generated: October 31, 2026

Formaldehyde → 4-(4-Bromobenzyl)-1-methylpiperidine

https://huagongshe.com/reaction/1888402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantHCID 20689421HCID 20689421—
SolventFormic AcidHCID 284—
Product4-(4-Bromobenzyl)-1-methylpiperidineHCID 5826684598.1%

Reaction Conditions

Temperature150 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-c5fb54bcd0554524bd9501c691cb2961
Source noteuspto-grants-2013_08