Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416031Generated: November 1, 2026

Anisole → HCID 22130792, compound

https://huagongshe.com/reaction/1416031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantSodium BicarbonateHCID 516892—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 22130072HCID 22130072—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 22130792HCID 2213079287%

Reaction Steps

To a solution of 1-benzyloxymethyl-2-t-butyldimethylsilyloxymethyl-5-(3-chlorophenylthio)imidazole (45)in nitromethane (108 ml)was added 14.7 g of (137 mmol)of anisole, and then, 18.1 g (136 mmol)of anhydrous aluminium chloride was gradually added at lower than 30° C. After completion of the addition, the mixture was stirred at room temperature for 15 minutes. The reaction mixture was cooled, and there were added water and a saturated aqueous sodium hydrogen carbonate solution to be alkaline. Ethyl acetate was added to the mixture, and the mixture was filtered on Hiflow Super Cell to separate. The organic layer was washed with water, dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by silica gel chromatography (7% methanol-methylene chloride) to give 9.5 g of [5-(3-chlorophenylthio)-1H-imidazol-2-yl]methanol as oil (yield 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05910506
Source datasetuspto-grants-1999_06
ORD IDord-b3a829f4e55944f89be165853b847606
Source noteuspto-grants-1999_06