HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702826Generated: October 26, 2026
Water → 1-(2,2-Dichloro-1,1-difluoroethoxy)-4-(4-(methylsulfonyl)phenoxy)benzene
https://huagongshe.com/reaction/1702826
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1,1-Dichloro-2,2-difluoroethene | HCID 6592 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phenol, 4-(4-(methylsulfonyl)phenoxy)- | HCID 514882 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(2,2-Dichloro-1,1-difluoroethoxy)-4-(4-(methylsulfonyl)phenoxy)benzene | HCID 13078519 | 89.4% |
Reaction Steps
To a solution of 5.29 g (0.0200 mole) of 4-(4-(methylsulfonyl)phenoxy)phenol (Example 21) in 100 ml of acetonitrile was added 0.80 g (0.0200 mole) of NaOH. The mixture was stirred at room temperature for 1 hr and then cooled to 3° C. in an ice bath. To the cold slurry was slowly added 4.0 g (0.0300 mole) of 1,1-difluoro-2,2-dichloroethylene dissolved in 15 ml of acetonitrile and the reaction mixture stirred at 3°-5° C. for 3 hrs. To the cold mixture 150 ml of water was added which resulted in the product precipitating as an oil. The product was extracted from the mixture with CH2Cl2. The organic layer was washed with water, dried (Na2SO4) and solvent rmoved in vacuo, which gave 7.1 g (89.4% yield) of product. Purification was accomplished by column chromatography using silica gel as the support and chloroform as the eluent, which afforded purified 1 -(2,2-dichloro-1,1-difluoroethoxy)-4-(4-(methylsulfonyl)phenoxy)benzene, mp 67°-70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04349568 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-2a7878b900994793bddac7352bafc1b2 |
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| Source note | uspto-grants-1982_09 |
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