HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 68783444, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | tert-Butyl 4-(1H-benzimidazol-2-yl)piperidine-1-carboxylate | HCID 54672426 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 68783444 | HCID 68783444 | — |
Reaction Steps
The tert-butyl 4-(1H-benzimidazol-2-yl)piperidine-1-carboxylate (50.0 mg, 0.166 mmol) was dissolved in 2 mL of acetone with freshly ground potassium hydroxide (46.4 mg, 0.830 mmol). The mixture was stirred for 10 minutes at ambient temperature, and then methyl iodide (11.4 μL, 0.183 mmol) was added. After 10 minutes, the reaction was quenched by adding saturated aqueous ammonium chloride solution (10 mL). The sample was diluted with EtOAc (3×30 mL), washed with water (2×20 mL), and washed with brine (2×20 mL). The organic layer was dried over sodium sulfate, filtered, concentrated to give tert-butyl 4-(1-methyl-1H-benzimidazol-2-yl)piperidine-1-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08288409B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-73d5cce406944c3ca0b4012906135592 |
| Source note | uspto-grants-2012_10 |