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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392350Generated: October 30, 2026

Chloroform → HCID 22247880, compound

https://huagongshe.com/reaction/392350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantHydrofluoric AcidHCID 14917—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 6-amino-3-methoxy-2-pyrazinecarboxylateHCID 22662843—
ReactantSodium NitriteHCID 23668193—
SolventPyridineHCID 1049—
ProductHCID 22247880HCID 22247880—

Reaction Steps

In 140 mL of 70% solution of hydrogen fluoride in pyridine was dissolved 17.3 g of methyl 6-amino-3-methoxy-2-pyrazinecarboxylate at an ice-cooled temperature. Then, 7.8 g of sodium nitrite was added at −50° C. in three portions. After the foaming had ceased, the temperature was slowly elevated, and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was poured into a mixture of 300 mL of ice and 200 mL of chloroform, the deposited insoluble matter was filtered off, and then the organic layer was separated. The remaining aqueous layer was extracted with ten portions of chloroform, provided that the total quantity of liquid came to 500 mL. The organic layers thus obtained were united, pH was adjusted to 7 with a saturated aqueous solution of sodium hydrogen carbonate, and the organic layer was separated. The organic layer thus obtained was washed with saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel chromatography [eluent: n-hexane:ethyl acetate=4:1] to obtain 14.3 g of methyl 6-fluoro-3-methoxy-2-pyrazinecarboxylate as a solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800629B2
Source datasetuspto-grants-2004_10
ORD IDord-c73d3d3497cc4a65a20f2d5ca77cabcf
Source noteuspto-grants-2004_10