HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1182637Erstellt: 25. Oktober 2026
Pivaloyl chloride → 2-Bromo-2,2-difluoroethyl pivalate
https://huagongshe.com/reaction/1182637
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pivaloyl chloride | HCID 62493 | — |
| Edukt | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Edukt | 2-Bromo-2,2-difluoroethan-1-ol | HCID 18368476 | — |
| Edukt | 1,1-Difluoro-2-hydroxyethanesulfonate | HCID 57783303 | — |
| Produkt | 2-Bromo-2,2-difluoroethyl pivalate | HCID 57817345 | — |
Reaktionsschritte
On the other hand, the 1,1-difluoro-2-hydroxyethanesulfonate of the general formula (17) can be prepared by reducing ethyl bromodifluoroacetate to 2-bromo-2,2-difluoroethanol, esterifying the 2-bromo-2,2-difluoroethanol with pivaloyl chloride to form 2-bromo-2,2-difluoroethyl pivalate, sulfinating the 2-bromo-2,2-difluoroethyl pivalate to form 1,1-difluoro-2-(pivaloyloxy)ethanesulfinate, oxidizing the 1,1-difluoro-2-(pivaloyloxy)ethanesulfinate to 1,1-difluoro-2-(pivaloyloxy)ethanesulfonate, and then, saponifying the 1,1-difluoro-2-(pivaloyloxy)ethanesulfonate. Any known esterification technique can be adopted to react the carboxylic acid derivative of the general formula (16) and the 1,1-difluoro-2-hydroxyethanesulfonate of the general formula (17) for production of the polymerizable fluorine-containing sulfonate compound of the general formula (3) as indicated in SCHEME (1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08663897B2 |
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| Quelldatensatz | uspto-grants-2014_03 |
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| ORD ID | ord-0457debc529d4e0da241829e75df0a04 |
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| Quellennotiz | uspto-grants-2014_03 |
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