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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351178Erstellt: 26. Oktober 2026

Chloroacetic Acid → 2-(Chloromethyl)-5,6-dimethyl-1h-benzimidazole

https://huagongshe.com/reaction/351178

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetic AcidHCID 300—
EduktSodium CarbonateHCID 10340—
Edukt4,5-Dimethyl-1,2-phenylenediamineHCID 76635—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelWaterHCID 962—
Produkt2-(Chloromethyl)-5,6-dimethyl-1h-benzimidazoleHCID 26628054,5%

Reaktionsschritte

To a stirred solution of 4,5-dimethylphenylene-1,2-diamine (680 mg, 5 mmol) in 4N HCl (12 mL) was added chloroacetic acid (940 mg, 10 mmol). The solution was then heated to reflux for 17 hours, then cooled to room temperature. Solid sodium carbonate was then added slowly, with stirring, until the pH of the solution was approximately 9.0, at which point a beige precipitate formed. The aqueous phase was then diluted with water (10 mL) and extracted repeatedly with ethyl acetate. The combined organic fractions were then dried, concentrated and the residue was purified by column chromatography on silica gel (10% MeOH in CH2Cl2) to afford the desired 2-(chloromethyl)-5,6-dimethylbenzimidazole (530 mg, 54%). 1H NMR (CDCl3) δ 1.59 (br s, 1H), 2.31 (s, 6H), 4.83 (s, 2H), 7.42 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07183273B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-263aa6ba2d364930bfb76f9c2d88b47f
Quellennotizuspto-grants-2007_02