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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728188Generated: November 1, 2026

Dimethylformamide → 3-chloro-5-formyl-2H-pyridine-1-carboxylic acid phenyl ester

https://huagongshe.com/reaction/1728188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPotassium AcetateHCID 517044—
Reactant3-chloro-2H-pyridine-1-carboxylic acid phenyl esterHCID 57565901—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-chloro-5-formyl-2H-pyridine-1-carboxylic acid phenyl esterHCID 5756593196.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Phosphorus oxychloride (5.4 g, 57.9 mmol) was added slowly to a stirred solution of DMF (8.9 mL, 116 mmol) in dichloromethane (10 mL) at 0° C. After addition, the solution was stirred at same temperature for 25 min., then transferred a solution of 3-chloro-2H-pyridine-1-carboxylic acid phenyl ester (5.67 g, 26.3 mmol) in anhydrous dichloromethane (50 mL) at 0° C. The ice bath was removed and stirring was continued at r.t. for 2 h, then the mixture was refluxed for 40 min. After the mixture was cooled to 0° C., an aqueous solution of KOAc (15 g, 153 mmol) in water (50 mL) was added slowly. The mixture was refluxed for 20 min., organic layer was separated, and aqueous layer was extracted with dichloromethane (50 mL). The organic layers were combined, washed with saturated NaHCO3, water and brine then dried over MgSO4, concentrated to give the crude product (Yield: 6.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-2d965dbf63c241e483c8dc30a2df0a20
Source noteuspto-grants-2009_02