HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pivaloyl chloride → 2-Bromo-2,2-difluoroethyl pivalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | 2-Bromo-2,2-difluoroethan-1-ol | HCID 18368476 | — |
| Product | 2-Bromo-2,2-difluoroethyl pivalate | HCID 57817345 | — |
Reaction Steps
These recurring units may be synthesized, for example, by the following method. One exemplary compound may be synthesized by reacting 2-bromo-2,2-difluoroethanol with pivalic chloride or anhydride to form 2-bromo-2,2-difluoroethyl pivalate, converting the bromo group into sodium sulfinate using a sulfur compound such as sodium dithionite, and converting sulfinic acid into sulfonic acid using an oxidizing agent such as hydrogen peroxide. This is followed by cation exchange with a triarylsulfonium halide or the like. The pivalic ester is then subjected to alkaline hydrolysis. Through reaction with (meth)acrylic anhydride, the alcohol resulting from hydrolysis is converted into a (meth)acrylic derivative, yielding the end compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048610B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-62a0d45137b84955ba426b84f030d4bd |
| Source note | uspto-grants-2011_11 |