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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587895Generated: October 27, 2026

Hydrochloric Acid → Methyl 5-(2-ethoxy-1,1-difluoro-2-oxoethyl)pyrazine-2-carboxylate

https://huagongshe.com/reaction/587895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantTriglymeHCID 8189—
ReactantEthyl bromodifluoroacetateHCID 69585—
ReactantBromotrimethylsilaneHCID 76113—
ReactantMethyl 5-bromopyrazine-2-carboxylateHCID 27282430—
CatalystZincHCID 23994—
CatalystCopper bromide (CuBr2)HCID 24611—
SolventTolueneHCID 1140—
SolventDimethylacetamideHCID 31374—
ProductMethyl 5-(2-ethoxy-1,1-difluoro-2-oxoethyl)pyrazine-2-carboxylateHCID 117965522—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of zinc powder (4.58 g, 0.070 mol) and triglyme (35 mL) was added TMSBr (0.91 mL, 0.007 mol) under nitrogen, and the mixture was stirred at 70° C. for 1.5 h. After the mixture was cooled to room temperature, ethyl bromodifluoroacetate (10.8 mL, 0.084 mol) was added while maintaining the internal temperature at 22 to 27° C., and the mixture was stirred at 20° C. for 30 min and then cooled to 0° C. After addition of the solution of methyl 5-bromopyrazine-2-carboxylate (II, 7.23 g, 0.033 mol) in DMA (106 mL) to the mixture, the resulting mixture was warmed to 20° C. Copper bromide (CuBr, 10.0 g, 0.070 mol) was added in fifth portions over 1 h followed by stirring the mixture for 30 min. The reaction mixture was transferred into a pre-cooled (ice bath) mixture of an aqueous sodium chloride solution (6.3%, 111 g), concentrated hydrochloric acid (29.4 mL) and toluene (140 mL), and the resulting mixture was vigorously stirred. The organic layer was separated and washed twice with aqueous sodium chloride solutions (5.7%, 70 g and 2.9%, 70 g) to afford 136 g of a toluene solution of methyl 5-(2-ethoxy-1,1-difluoro-2-oxoethyl)pyrazine-2-carboxylate (III).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227942B2
Source datasetuspto-grants-2016_01
ORD IDord-5dd01851ab7c4caebcf8bfdbabc724e0
Source noteuspto-grants-2016_01