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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1096955Erstellt: 25. Oktober 2026

Oxalyl chloride → Methyl 2-(benzyloxy)-6-chloroisonicotinate

https://huagongshe.com/reaction/1096955

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt2-Chloro-6-benzyloxypyridine-4-carboxylic acidHCID 2762508—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelChloroformHCID 6212—
ProduktMethyl 2-(benzyloxy)-6-chloroisonicotinateHCID 57930944—

Reaktionsschritte

With cooling with ice, oxalyl chloride (5.8 mL) and DMF (3 drops) were added to a CHCl3 (40 mL) solution of 2-chloro-6-benzyloxypyridine-4-carboxylic acid, and stirred at that temperature for 1 hour. DMF (3 drops) was added to it, and stirred overnight at room temperature, then oxalyl chloride (2.9 mL) and DMF (3 drops) were added to it, and stirred at room temperature for 3 hours. The solvent was evaporated away, CHCl3-MeOH was added to the residue, and stirred at room temperature for 30 minutes. Sodium bicarbonate water was added to the reaction solution, extracted with chloroform, and the organic layer was washed with water, saturated sodium bicarbonate water and saturated saline water, and dried with anhydrous sodium sulfate. This was filtered, concentrated under reduced pressure, and the residue was purified through silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08138197B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-0a63c435e4e145fc96800427431caea7
Quellennotizuspto-grants-2012_03