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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505917Generated: November 2, 2026

Formaldehyde → 4-(3-Bromophenyl)-1-methylpiperidine

https://huagongshe.com/reaction/1505917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactanttert-Butyl 4-(3-bromophenyl)piperidine-1-carboxylateHCID 40425223—
SolventFormic AcidHCID 284—
Product4-(3-Bromophenyl)-1-methylpiperidineHCID 5340784299.3%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 4-(3-bromophenyl)-1-N-Boc piperidine (430 mg, 1.26 mmol), formic acid (5 mL) and formaldehyde (0.5 mL) was heated under microwave irradiation at 150° C. for 10 minutes. The cooled reaction mixture was loaded onto a 70 g SCX-2 cartridge which was washed with methanol (200 mL) and then eluted with 2N ammonia in methanol (200 mL). Concentration of the combined basic fractions in vacuo afforded the title compound (318 mg, 99%) as a brown oil. 1H NMR (CDCl3, 300 MHz): 7.38-7.36 (m, 1H); 7.35-7.29 (m, 1H); 7.17-7.14 (m, 2H); 3.03-2.92 (m, 2H); 2.52-2.37 (m, 1H); 2.32 (s, 3H); 2.10-1.99 (m, 2H); 1.87-1.69 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-861815beb0eb48c7bd5abe29508ab513
Source noteuspto-grants-2015_12