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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953404Generated: October 29, 2026

Ammonium formate → 3-[(E)-2-(3-aminophenyl)vinyl]-5-bromopyridine

https://huagongshe.com/reaction/1953404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant3-bromo-5-[(E)-2-(3-nitrophenyl)vinyl]pyridineHCID 23298125—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3-[(E)-2-(3-aminophenyl)vinyl]-5-bromopyridineHCID 2329809071.3%

Reaction Steps

A mixture of 3-bromo-5-[(E)-2-(3-nitrophenyl)vinyl]pyridine (5.55 g), iron powder (3.05 g) and ammonium formate (5.73 g) in ethanol (90 ml) and water (30 ml) was stirred at 90pbC. for 30 minutes. The mixture was filtered while hot. The filtrate was added to sodium bicarbonate solution and extracted with ethyl acetate twice. The combined organic solution was washed with sodium bicarbonate solution and brine, dried over magnesium sulfate and concentrated to give 3-[(E)-2-(3-aminophenyl)vinyl]-5-bromopyridine (3.57 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117875
Source datasetuspto-grants-2000_09
ORD IDord-42dfc52151bd4790bacaafcbd35d61f8
Source noteuspto-grants-2000_09