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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493325Generated: November 2, 2026

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

https://huagongshe.com/reaction/1493325

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 g 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 l 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 numberUS05021443
Source datasetuspto-grants-1991_06
ORD IDord-c9d389c812e3401aa8ea85d136467d18
Source noteuspto-grants-1991_06