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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982847Generated: November 2, 2026

Hydrochloric Acid → HCID 21909267, compound

https://huagongshe.com/reaction/1982847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 68873227HCID 68873227—
SolventDichloromethaneHCID 6344—
ProductHCID 21909267HCID 21909267—

Reaction Steps

To a solution of 3-benzyloxy-4-(4-ethylbenzyl)benzyl alcohol (0.87 g) in dichloromethane (20 mL) were added triethylamine (0.44 mL) and methanesulfonyl chloride (0.22 mL) at 0° C., and the mixture was stirred for 2 hours. To the reaction mixture was added 0.5 mol/L hydrochloric acid, and the mixture was extracted with diethyl ether. The organic layer was washed with water and a saturated aqueous sodium hydrogen carbonate, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was dissolved in dimethylsulfoxide (10 mL), and potassium cyanide (0.68 g) and a catalytic amount of sodium iodide were added to the solution. The mixture was stirred at 80° C. for 12 hours. To the reaction mixture was added water, and the mixture was extracted with diethylether. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate=5/1-3/1) to give [3-benzyloxy-4-(4-ethylbenzyl)phenyl]-acetonitrile (0.41 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541341B2
Source datasetuspto-grants-2009_06
ORD IDord-cc66590a353e411289e0262925249193
Source noteuspto-grants-2009_06