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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888454Generated: November 4, 2026

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

https://huagongshe.com/reaction/1888454

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 numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-f5eb7fe41b2043849c1e3c7136da77b3
Source noteuspto-grants-2013_08