HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyldiazomethane → methyl 1H-1,3-benzodiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 5-Benzimidazolecarboxylic acid | HCID 459456 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | methyl 1H-1,3-benzodiazole-5-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06498165B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-f766d6e5d79b4fc291a27aa69e3651f8 |
| Source note | uspto-grants-2002_12 |