Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505643Generated: October 29, 2026

1-Methylimidazole → HCID 59031741, compound

https://huagongshe.com/reaction/505643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantSodium ThiosulfateHCID 24477—
ReactantHCID 13222891HCID 13222891—
ReactantSodium HypochloriteHCID 23665760—
SolventEthyl AcetateHCID 8857—
ProductHCID 59031741HCID 5903174178%

Reaction Steps

To a solution (50 mL) of ethyl acetate containing 2,2,8-trimethyl-7-nitro-2H-1-benzopyran (3.32 g, 15.1 mmol), N-methyl imidazole (0.482 mL, 6.05 mmol) and (R,R,S,S)-Ph,Ph salen manganese complex (XY) (142 mg, 0.151 mmol) were added at room temperature, and sodium hypochlorite aqueous solution (34.1 mL, 1.776 mol/kg, 60.5 mmol) was added dropwise, and the resulting mixture was stirred at room temperature for 1 hour. Upon the completion of the reaction, sodium thiosulfate aqueous solution was added to the reaction solution, the resulting solution was filtered through celite. The resulting filtrate extracted with ethyl acetate. The organic phase was washed with water and sodium chloride aqueous solution, and then dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by column chromatography (hexane/ethyl acetate=7/1) and the aimed product was obtained as pale yellow crystal (yield: 78%, optical purity: 99% ee).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781483B2
Source datasetuspto-grants-2010_08
ORD IDord-b0a1d4787b69411184243abdf1fcc4c4
Source noteuspto-grants-2010_08