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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358985Generated: October 30, 2026

Citric Acid → HCID 58336831, compound

https://huagongshe.com/reaction/2358985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantSodium ChlorideHCID 5234—
Reactant2,6-DibromopyridineHCID 12274—
ReactantSodium HydroxideHCID 14798—
ReactantAcetamide, 2-methoxy-N,N-dimethyl-HCID 11126230—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 58336831HCID 58336831—

Reaction Conditions

Temperature30 °C

Reaction Steps

14.5 g (61.2 mmol) of 2,6-dibrompyridine were dissolved in about 50 ml of THF, and 35 ml of 2 M isopropylmagnesium chloride (corresponds to 70 mmol) were added under argon. The temperature of the mixture increased. The mixture was stirred at room temperature for another 1.5 h and at 30° C. for 2 h and then cooled in a CO2/EtOH bath, and a solution of 8 g (68.2 mmol) of 2-methoxy-N,N-dimethylacetamide in THF was added, the thickened reaction material was diluted with more THF and allowed to thaw, ethyl acetate, aq. citric acid, dil. aqueous sodium hydroxide solution to pH=6, aq. NaCl were added, the aqueous phase was extracted three times with ethyl acetate and the combined organic phases were dried with MgSO4 and concentrated by evaporation. The residue was distilled under reduced pressure in a kugelrohr and the distillate was recrystallized from a little benzotrifluoride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685964B2
Source datasetuspto-grants-2014_04
ORD IDord-f8f987e797fe446695ab0f22ac4ceddf
Source noteuspto-grants-2014_04