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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051542Generated: October 26, 2026

Methyl iodide → Methyl 1-methyl-1H-benzo[d]imidazole-5-carboxylate

https://huagongshe.com/reaction/1051542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 1H-1,3-benzodiazole-5-carboxylateHCID 2779733—
ReactantMethyl 1-methyl-1H-benzo[d]imidazole-6-carboxylateHCID 10583823—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 1-methyl-1H-benzo[d]imidazole-5-carboxylateHCID 96531978%

Reaction Steps

A solution of methyl 1H-benzo[d]imidazole-6-carboxylate (9.5 g, 53.9 mmol) in THF (100 mL) had NaH (2.59 g, 64.7 mmol) added at 0° C. After stirring for 30 min, CH3I (13.23 g, 93.2 mmol) was added and the mixture was stirred at room temperature for 1 h. The reaction was then quenched by addition of water and extracted with DCM (3×100 mL). The combined organic layers were dried over Na2SO4 and concentrated to give a mixture of two isomeric products methyl 1-methyl-1H-benzo[d]imidazole-6-carboxylate and methyl 1-methyl-1H-benzo[d]imidazole-5-carboxylate (8.0 g, Yield 78%). LCMS (m/z): 191.06 (M+1). This crude mixture was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388173B2
Source datasetuspto-grants-2016_07
ORD IDord-095faa01399a4735bfb4e66fe47b0307
Source noteuspto-grants-2016_07