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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028482Generated: October 25, 2026

Formaldehyde → Diethyl 1H-imidazole-4,5-dicarboxylate

https://huagongshe.com/reaction/1028482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium AcetateHCID 517165—
ReactantDiethyl tartrateHCID 6993580—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
ProductDiethyl 1H-imidazole-4,5-dicarboxylateHCID 350670—

Reaction Steps

To a solution of L-tartaric acid diethyl ester (2.0 g) in ethyl acetate (34.2 ml), 1,3-dibromo-5,5-dimethylhydantoin (3.3 g) was added, and the reaction solution was stirred at room temperature for 3 hours. To the reaction solution, acetic acid (17 ml) was added, and subsequently 36% aqueous formaldehyde solution (3.45 ml) was added under ice cooling at the internal temperature of 10° C. or below, followed by addition of ammonium acetate (17.2 g) at an internal temperature of 10° C. or below. The reaction solution was stirred at room temperature for 30 minutes, followed by stirring at 50° C. for 3 hours. To the reaction solution, 5N sodium hydroxide was added, and the aqueous layer was extracted with ethyl acetate. The organic layers were combined, and dried over magnesium sulfate. Quantitative analysis of the resulting ethyl acetate solution by HPLC showed that the title compound was not produced. The condition for HPLC analysis was identical with that for Example 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735598B2
Source datasetuspto-grants-2014_05
ORD IDord-e512cbfe24dc4a7593040cf9a99cb8f7
Source noteuspto-grants-2014_05