HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489431Generated: October 31, 2026
1,3-Difluorobenzene → HCID 10527851, compound
https://huagongshe.com/reaction/1489431
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Difluorobenzene | HCID 9741 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 86751397 | HCID 86751397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10527851 | HCID 10527851 | — |
Reaction Steps
(2R)-2-[3-[4-(2,2,3,3-Tetrafluoropropoxy)phenyl]-2,3-dihydro-2-oxo-1H-imidazol-1-yl]propanoyl chloride (1.5 g) was dissolved in 30 ml of dichloromethane, to which 3.8 ml of 1,3-difluorobenzene and 2.3 g of anhydrous aluminum chloride (powder) were added. The mixture was refluxed with heating for 5 hours. The reaction solution was cooled, poured into 100 ml of ice water and extracted with 100 ml of ethyl acetate. The extract was washed with 50 ml of 1N-hydrochloric acid and 50 ml of a saturated aqueous solution of sodium chloride successively, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (silica gel: 50 g, eluent; hexane:ethyl acetate:acetic acid=2:1:0.03) and crystallized from 10 ml of diisopropyl ether to give 0.25 g of 1-[(1R)-2-(2,4-difluorophenyl)-2-oxo-1-methylethyl]-3-[4-(2,2,3,3-tetrafluoropropoxy)phenyl]-2(1H,3H)-imidazolone as colorless powdery crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05677464 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-970c40c6387746b8a3ad9bdf20678bf5 |
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| Source note | uspto-grants-1997_10 |
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