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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610833Generated: November 1, 2026

Acetaldehyde → HCID 22258232, compound

https://huagongshe.com/reaction/1610833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantAmmoniaHCID 222—
ReactantSodium ChlorideHCID 5234—
ReactantAmmonium AcetateHCID 517165—
Reactant3-Methylcyclohexane-1,2-dioneHCID 3321360—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 22258232HCID 2225823243.3%

Reaction Steps

20.0 g (0.159 mol) of 3-Methyl-1,2-cyclohexanedione and 183.31 g (2.38 mol) of ammoniumacetate are dissolved in 760 ml DMSO. A solution of 27.94 g (0.34 mol) acetaldehyde dissolved in 40 ml DMSO is dropped to the reaction mixture. The reaction is heated for 20 minutes to 40° C., 20 minutes to 60° C. and 40 minutes to 80° C. The reaction is allowed to cool down to rt. 2.5 l saturated sodium chloride solution and ammonia are added to reach a pH of 8-9. The solution is extracted with ethyl acetate and the organic phases are dried over sodium sulfate. The solvent is evaporated under vacuum. The crystalls are filtrated and washed with ethyl acetate and diethyl ether to yield 10.3 g (43.3% of th.) 2,4-Dimethyl-4,5,6,7-tetrahydro-1H-benzimidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984646B2
Source datasetuspto-grants-2006_01
ORD IDord-f9765ab7993941fe9dd4be146d30532a
Source noteuspto-grants-2006_01