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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653669Generated: October 26, 2026

O-Phenylenediamine → Ethyl 4-(benzimidazol-2-yl)-3,3-dimethylbutanoate

https://huagongshe.com/reaction/653669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
ReactantTriethylamineHCID 8471—
Reactant2-Methyl-2-buteneHCID 10553—
Reactant3,3-Dimethylglutaric acidHCID 20984—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(benzimidazol-2-yl)-3,3-dimethylbutanoateHCID 14953059—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 139.2 of the acid chloride ethyl ester of 3,3-dimethylglutaric acid, prepared in Example 28, in 125 ml of chloroform, stabilized with amylene, is added dropwise, at a temperature of between 5° C. and 10° C., to a solution of 72.8 g of orthophenylenediamine and 112 ml of triethylamine in 1 l of anhydrous tetrahydrofuran. The mixture is stirred at 0° C. for two hours and then at 50° C. for one hour; the crystals are filtered off and the solvents are evaporated off under vacuum. The residue is taken up in 4.4 1 of ethanol and 444 ml of concentrated hydrochloric acid and the mixture is refluxed for 12 hours. The solvents are evaporated off and the residue is taken up with water and then neutralized with a 1 N solution of sodium hydroxide and extracted with ether. The ether phase is dried and then evaporated under vacuum to give 99 g of ethyl 4-(benzimidazol-2-yl)-3,3-dimethylbutanoate in the form of crystals melting at 123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05128359
Source datasetuspto-grants-1992_07
ORD IDord-51a1ea20883245288355eda4ce600edf
Source noteuspto-grants-1992_07