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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063930Generated: November 1, 2026

Methyl iodide → HCID 68783444, compound

https://huagongshe.com/reaction/2063930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
Reactanttert-Butyl 4-(1H-benzimidazol-2-yl)piperidine-1-carboxylateHCID 54672426—
SolventAcetoneHCID 180—
ProductHCID 68783444HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288409B2
Source datasetuspto-grants-2012_10
ORD IDord-73d5cce406944c3ca0b4012906135592
Source noteuspto-grants-2012_10