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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281885Generated: October 31, 2026

Hydrochloric Acid → HCID 178498030, compound

https://huagongshe.com/reaction/2281885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantAcetylacetoneHCID 31261—
ReactantHCID 86653286HCID 86653286—
ProductHCID 178498030HCID 17849803059%

Reaction Steps

Add 2N hydrochloric acid (8 mL) to a solution of 3,4-diamino-5-chlorobenzoate (from acid preparation 1, 435 mg, 2.17 mmol) in ethanol (20 mL). Heat the mixture to reflux then add acetylacetone (437 mg, 4.37 mmol) to the yellow solution. The yellow solution turned purple upon addition. Stir at reflux for 1 hour and the solution turned back to yellow. Stir at reflux for an additional 1 hour. Concentrate the solvent to a colorless residue. Add water (20 mL). Extract the suspension with ethyl acetate (20 mL). Basify the aqueous layer with 2N sodium hydroxide (˜8 mL) to pH˜10. Extract with ethyl acetate (3×15 mL). Wash combined organics from the basic extraction with brine (5 mL). Dry over magnesium sulfate, filter, concentrate, and dry under high vacuum to yield methyl 7-chloro-2-methyl-1H-benzo[d]imidazole-5-carboxylate (290 mg, 59%) as a colorless solid. 1H NMR (400 MHz, CDCl3) δ ppm 2.68 (s, 3 H), 3.93 (s, 3 H), 7.25 (s, 1 H), 7.96 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139587B2
Source datasetuspto-grants-2015_09
ORD IDord-e4e4bb4871c542f4a164c2aa08c403d2
Source noteuspto-grants-2015_09