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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64408Generated: October 26, 2026

Ethanol → Methyl 6-amino-5-[(2-fluorobenzyl)oxy]nicotinate

https://huagongshe.com/reaction/64408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 5-[(2-fluorobenzyl)oxy]-6-nitronicotinateHCID 86713415—
CatalystIronHCID 23925—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 6-amino-5-[(2-fluorobenzyl)oxy]nicotinateHCID 8671341699.8%

Reaction Steps

To a solution of 2.5 g of methyl 5-[(2-fluorobenzyl)oxy]-6-nitronicotinate in 25 ml of THF were added 50 ml of ethanol, 25 ml of water, 218 mg of ammonium chloride, and 1.37 g of iron, followed by heating to reflux for 2 hours. After leaving to be cooled at room temperature, the reaction mixture was filtered over Celite, and to the filtrate were added a saturated aqueous sodium hydrogen carbonate solution and chloroform to carry out a layer separation operation. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to obtain 2.25 g of methyl 6-amino-5-[(2-fluorobenzyl)oxy]nicotinate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447090B2
Source datasetuspto-grants-2016_09
ORD IDord-aea80e7c2e7244078ef4af820641ff21
Source noteuspto-grants-2016_09