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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579704Generated: October 30, 2026

Benzyl Chloride → HCID 20136108, compound

https://huagongshe.com/reaction/579704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium hydrideHCID 24758—
ReactantHCID 20136111HCID 20136111—
SolventAcetonitrileHCID 6342—
ProductHCID 20136108HCID 20136108—

Reaction Conditions

Temperature5 °C

Reaction Steps

16.1 g (0.05 mol) of 4-hydroxy-1-methyl-3-[3-methyl-4-(1,1,2,2-tetrafluoroethoxy)phenyl]imidazolidin-2-one are dissolved in 150 ml of acetonitrile, and 1.50 g of sodium hydride (80% strength in white oil) are added at 5° C. The mixture is stirred for 10 minutes at 5° C., and 6.40 g (0.05 mol) of benzyl chloride are subsequently added dropwise at 5° C. The mixture is stirred for 5 hours at 50°and poured into 400 ml of ice-water. The mixture is extracted twice with 100 ml of methylene chloride in each case, and the combined methylene chloride phases are washed with 100 ml of water and dried over sodium sulfate. After removing the solvent by distillation, 19.4 g (94% of theory) of 4-benzyloxy-1-methyl-3-[3-methyl-4-(1,1,2,2-tetrafluoroethoxy)phenyl]imidazolidin-2-one are obtained in the form of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04749403
Source datasetuspto-grants-1988_06
ORD IDord-33a281bcfbca4ff1a2a0f69e443ebaf0
Source noteuspto-grants-1988_06