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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405010Generated: October 26, 2026

Hydrochloric Acid → 2-Bromo-2,2-difluoroethyl pivalate

https://huagongshe.com/reaction/405010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropyl EtherHCID 7914—
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
Reactant2-Bromo-2,2-difluoroethan-1-olHCID 18368476—
SolventWaterHCID 962—
Product2-Bromo-2,2-difluoroethyl pivalateHCID 5781734588.7%

Reaction Steps

A glass flask equipped with a thermometer, a condenser and a dropping funnel was charged with 271 g (2.24 moles) of pivaloyl chloride, 360 g (2.23 moles) of 2-bromo-2,2-difluoroethanol and 1.5 L of diisopropyl ether, followed by stirring. Then, 318 g (3.14 moles) of triethylamine was added dropwise thereto, in an iced bath. After the termination of the dropping, stirring was conducted for 1 hour at room temperature. Then, the termination of the reaction was confirmed by gas chromatography. With the addition of 300 mL of water, a reaction solution was completely dissolved therein, followed by adding 500 mL of 2N hydrochloric acid thereto. The reaction solution was separated into an organic layer and a water layer, followed by extracting the water layer with 500 ml of diisopropyl ether. Subsequently, the organic layer was rinsed with 500 ml of saturated brine, followed by drying with anhydrous sodium sulfate. Thereafter, a solvent was distilled off, thereby obtaining 485 g (82% yield, 93% purity) of 2-bromo-2,2-difluoroethyl pivalate in the form of a light yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748672B2
Source datasetuspto-grants-2014_06
ORD IDord-88f352f510b0436e8ed7d3da8ab8e6bb
Source noteuspto-grants-2014_06