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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408761Generated: November 2, 2026

Methyl iodide → HCID 58423762, compound

https://huagongshe.com/reaction/1408761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178423433HCID 178423433—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58423762HCID 5842376290.3%

Reaction Steps

NaH (5.3 mg, 0.131 mmol) is added to a solution of 2′-amino-6-bromo-2,2-dimethyl-spiro[chroman-4,4′-imidazol]-5′(3′H)-one (45 mg, 0.131 mmol) in THF (3 mL) at 0° C. under N2. The mixture is stirred for 1 h at room temperature. Then MeI (18.6 mg, 0.131 mmol) is added. The mixture is quenched with water and extracted with ethyl acetate. The organic layer is concentrated in vacuo. The residue is purified by preparative TLC to give 2′-amino-6-bromo-1′,2,2-trimethylspiro[chroman-4,4′-imidazol]-5′(1′H)-one (40 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921359B2
Source datasetuspto-grants-2014_12
ORD IDord-d3be12240e434623b40ab1bcb928f47e
Source noteuspto-grants-2014_12