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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389111Generated: October 30, 2026

Dichloromethane → HCID 22961979, compound

https://huagongshe.com/reaction/389111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantHCID 178497375HCID 178497375—
SolventWaterHCID 962—
ProductHCID 22961979HCID 2296197971.3%

Reaction Steps

Triethylamine (4.7 ml) and chlorotriphenylmethane (9.37 g) were added to a mixture of methyl 4,5,6,7-tetrahydro-1H-benzimidazole-5-carboxylate (6.73 g) and dichloromethane (70 ml), followed by stirring at room temperature overnight. Water was added to the reaction solution, followed by extraction with dichloromethane, the organic layer was concentrated, and the resulting residue was purified by silica gel column chromatography (chloroform) to obtain a mixture (10.13 g) of methyl 1-trityl-4,5,6,7-tetrahydro-1H-benzimidazole-5-carboxylate and methyl 1-trityl-4,5,6,7-tetrahydro-1H-benzimidazole-6-carboxylate. Methanol (50 ml), water (20 ml) and sodium hydroxide (4.78 g) were added to the obtained mixture, followed by heating to reflux overnight. The reaction solution was concentrated, water and concentrated hydrochloric acid (8 ml) were added to the residue, and the precipitated solid was collected by filtration, washed with water and acetone and dried under reduced pressure to obtain a mixture (7.07 g) of 1-trityl-4,5,6,7-tetrahydro-1H-benzimidazole-5-carboxylic acid and 1-trityl-4,5,6,7-tetrahydro-1H-benzimidazole-6-carboxylic acid, as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377923B2
Source datasetuspto-grants-2013_02
ORD IDord-2addf12291174ee58c34b9e86e2e959a
Source noteuspto-grants-2013_02