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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225619Generated: October 31, 2026

Thionyl Chloride → 4,5,6,7-Tetrahydro-1H-benzimidazole

https://huagongshe.com/reaction/2225619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4,5,6,7-Tetrahydrobenzimidazole-5-carboxylic acid sulfateHCID 14856795—
Solvent1,2-DichloroethaneHCID 11—
Product4,5,6,7-Tetrahydro-1H-benzimidazoleHCID 304263—

Reaction Conditions

Temperature30 °C

Reaction Steps

4,5,6,7-Tetrahydrobenzimidazole-5-carboxylic acid sulfate (1.32 g) was refluxed in 10 ml of 1,2-dichloroethane together with 1.78 g of thionyl chloride for 30 minutes, and the excess of thionyl chloride and the solvent were removed by distillation under reduced pressure. To the residue was added 10 ml of 1,2-dichloroethane, and 1.6 ml of indoline was added dropwise thereto at 30° C. or lower while stirring followed by stirring at room temperature for 2 hours. The reaction mixture was successively extracted once with 30 ml of water and twice with 20 ml of water. The combined aqueous layer was adjusted to a pH of 9 to 10 with a 10% sodium hydroxide aqueous solution and then extracted with methylene chloride. The combined methylene chloride layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was recrystallized from ethyl acetate to obtain 1.1 g (82.7%) of 5-(2,3-dihydroindol-1-yl)carbonyl]-4,5,6,7-tetrahydrobenzimidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344927
Source datasetuspto-grants-1994_09
ORD IDord-32f08c8d4abb456aa9c829f2f3866452
Source noteuspto-grants-1994_09