Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096574Generated: October 30, 2026

Methyl iodide → HCID 58423762, compound

https://huagongshe.com/reaction/2096574

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-dimethylspiro[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 numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-0b62fa3b076d40f0b636a0fdece336ab
Source noteuspto-grants-2013_05