HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579704Generated: October 30, 2026
Benzyl Chloride → HCID 20136108, compound
https://huagongshe.com/reaction/579704
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 20136111 | HCID 20136111 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20136108 | HCID 20136108 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04749403 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-33a281bcfbca4ff1a2a0f69e443ebaf0 |
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| Source note | uspto-grants-1988_06 |
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