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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487888Generated: October 25, 2026

Sodium Carbonate → N-((4-bromopyridin-2-yl)methyl)formamide

https://huagongshe.com/reaction/1487888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(4-Bromopyridin-2-yl)methanamineHCID 46907956—
SolventFormic AcidHCID 284—
ProductN-((4-bromopyridin-2-yl)methyl)formamideHCID 8607164965%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a 500-mL round-bottom flask, was placed (4-bromopyridin-2-yl)methanamine (compound 39.1, 8.0 g, crude) and formic acid (200 mL). The solution was stirred for 2 h at 100° C., then cooled and the pH was adjusted to 7 by careful and slow addition of aqueous sodium carbonate (sat.). The aqueous phase was extracted with ethyl acetate (3×200 mL) and the combined organic layers were washed with brine (3×30 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with ethyl acetate as the eluent to yield the title compound as a yellow oil (8.0 g, 90% pure, 65% yield over 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428502B2
Source datasetuspto-grants-2016_08
ORD IDord-4e8ffa804d234f16bd458b01b787537e
Source noteuspto-grants-2016_08