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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194271Generated: October 30, 2026

Carbon Dioxide → HCID 21269302, compound

https://huagongshe.com/reaction/1194271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 21269295HCID 21269295—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 21269302HCID 2126930263.5%

Reaction Steps

A solution of 3.3 parts of 1-(2,3-dihydro-2,2-dimethyl-4H-1-benzopyran-4-yl)-1H-imidazole-5-carboxylic acid in 45 parts in warm N,N-dimethylformamide was cooled to room temperature and then 2 parts of 1,1'-carbonylbis[1H-imidazole] were added. The whole was stirred at room temperature till CO2 evolution had ceased (±30 minutes). The mixture was heated to ±70° C. and 2.4 parts of ethanol and 0.1 parts of sodium ethoxide were added. Stirring was continued over weekend at ±70° C. After evaporation, the residue was taken up in water and trichloromethane. The organic layer was washed with water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using trichloromethane as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from hexane. The product was filtered off and dried, yielding 2.36 parts (63.5%) of ethyl 1-(2,3-dihydro-2,2-dimethyl-4H-1-benzopyran-4-yl)-1H-imidazole-5-carboxylate; mp. 80.9° C. (compound 1.138).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04813998
Source datasetuspto-grants-1989_03
ORD IDord-8db547f1fb40489a98a0024b765285d4
Source noteuspto-grants-1989_03