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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512168Generated: October 31, 2026

Methyl iodide → HCID 86716195, compound

https://huagongshe.com/reaction/512168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86716194HCID 86716194—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86716195HCID 8671619592.4%

Reaction Steps

To a solution of 3-cyclopropyl-2-(pyrimidin-5-yl)propanenitrile (1.5 g, 8.67 mmol) and MeI (1.45 g, 13.0 mmol) in 1,4-dioxane (20 ml) was added t-BuOK (9.57 ml, 9.57 mmol) dropwise at room temperature under N2. The mixture was stirred for 1 h at room temperature then quenched by sat.aq NH4Cl (20 ml) and extracted with EtOAc (3×30 ml). The organic layer was dried over Na2SO4 and concentrated under reduced pressure to give 3-cyclopropyl-2-methyl-2-(pyrimidin-5-yl)propanenitrile (1.5 g), which was used directly for next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102591B2
Source datasetuspto-grants-2015_08
ORD IDord-f9fd6ea0bee9444989e0cf7811310f22
Source noteuspto-grants-2015_08