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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1182637Erstellt: 25. Oktober 2026

Pivaloyl chloride → 2-Bromo-2,2-difluoroethyl pivalate

https://huagongshe.com/reaction/1182637

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPivaloyl chlorideHCID 62493—
EduktEthyl bromodifluoroacetateHCID 69585—
Edukt2-Bromo-2,2-difluoroethan-1-olHCID 18368476—
Edukt1,1-Difluoro-2-hydroxyethanesulfonateHCID 57783303—
Produkt2-Bromo-2,2-difluoroethyl pivalateHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08663897B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-0457debc529d4e0da241829e75df0a04
Quellennotizuspto-grants-2014_03