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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300793Generated: November 1, 2026

Trimethylsilyldiazomethane → methyl 1H-1,3-benzodiazole-5-carboxylate

https://huagongshe.com/reaction/2300793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant5-Benzimidazolecarboxylic acidHCID 459456—
SolventMethanolHCID 887—
Productmethyl 1H-1,3-benzodiazole-5-carboxylateHCID 2779733—

Reaction Steps

To a suspension of benzimidazole-5-carboxylic acid (100 mg, 0.616 mmol, 1 eq) in MeOH (4 mL) was added a 2N solution of trimethylsilyldiazomethane in hexanes (3×0.3 mL, 1.8 mmol, 3 eq). Nitrogen evolution was evident. Eventually a yellow color persisted. The reaction was quenched by the addition of a small amount of acetic acid. The MeOH was removed under reduced pressure and the mixture was purified by preparative thin layer chromatography (eluted with 7% MeOH in CH2Cl2) giving 66 mg of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498165B1
Source datasetuspto-grants-2002_12
ORD IDord-f766d6e5d79b4fc291a27aa69e3651f8
Source noteuspto-grants-2002_12