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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587898Generated: October 31, 2026

Hydrochloric Acid → 5-Difluoromethympyrazine-2-carboxylic acid

https://huagongshe.com/reaction/587898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
ReactantIsopropyl AcetateHCID 7915—
ReactantSodium HydroxideHCID 14798—
ReactantPotassiumHCID 5462222—
Reactant5-[Carboxy(difluoro)methyl]pyrazine-2-carboxylic acidHCID 72545421—
SolventWaterHCID 962—
Product5-Difluoromethympyrazine-2-carboxylic acidHCID 5746857564.2%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a mixture of potassium salt of 5-[carboxy(difluoro)methyl]pyrazine-2-carboxylic acid (IV, 1.00 g, 3.32 mmol) which was obtained from example (1-3)-B, isopropyl acetate (4 mL), and water (2 mL) were added concentrated sulfuric acid (0.60 mL, 10.8 mmol), and the organic layer was separated. The aqueous layer was re-extracted with isopropyl acetate (4 mL) followed by combining the obtained two organic layers. After stirring the mixture at 75° C. for 16.5 h, the mixture was stirred at 80° C. for 6 h and cooled to room temperature. After polish filtration of the mixture through a filter and rising the filter with isopropyl acetate (1 mL), water (4 mL) and aqueous sodium hydroxide solution (48%, 973 mg, 8.33 mmol) were added to the filtrate, and then the aqueous layer was separated. To the aqueous layer was added concentrated hydrochloric acid (0.83 mL, 10.0 mmol), and the resulting mixture was stirred while in ice-cooling for 17 h. The precipitated solids were collected by filtration, washed with water (0.5 mL), and dried at 50° C. under reduced pressure to afford the title compound (V, 371 mg, 64% yield) as pale brown solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227942B2
Source datasetuspto-grants-2016_01
ORD IDord-0def50fa63674ab78ada1647a6bccee0
Source noteuspto-grants-2016_01