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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532686Generated: October 30, 2026

Docosanoic Acid → 2-(2-Henicosyl-1H-benzimidazol-1-yl)-N,N-dimethyl-1-ethanamine

https://huagongshe.com/reaction/1532686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDocosanoic AcidHCID 8215—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantN-[2-(dimethylamino)ethyl]benzene-1,2-diamineHCID 522698—
SolventChloroformHCID 6212—
Product2-(2-Henicosyl-1H-benzimidazol-1-yl)-N,N-dimethyl-1-ethanamineHCID 2201375765.8%

Reaction Steps

Triethylamine (2.25 ml) was added to a suspension containing n-docosanoic acid (4.930 g) in chloroform (50 ml), and then ethyl chlorocarbonate (1.52 ml) was added thereto while being cooled with ice. After being stirred for 1.5 hours, a solution containing N-[2-(dimethylamino)ethyl]-1,2-benzenediamine (2.593 g) in chloroform (13 ml). After being stirred for 2.5 hours while being cooled with ice, the reaction mixture was diluted with chloroform, washed with saturated sodium hydrogencarbonate aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and concentrated. Concentrated hydrochloric acid (12.1 ml) was added to a solution containing the residue (8.644 g) in ethanol (87 ml). After being stirred for 2.5 hours at 90° C., the reaction mixture was concentrated. The residue, with ethyl acetate added thereto, was washed with 1N sodium hydroxide aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and concentrated. The residue (6.90 g) was purified by silica gel column chromatography (silica gel 150 g, chloroform:methanol=60:1-30:1), thereby yielding the entitled compound (4.604 g) as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204264B1
Source datasetuspto-grants-2001_03
ORD IDord-f29132af25534d71b0828b5b4d83bf23
Source noteuspto-grants-2001_03