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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | 2-Bromo-2,2-difluoroethan-1-ol | HCID 18368476 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-2,2-difluoroethyl pivalate | HCID 57817345 | 88.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748672B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-88f352f510b0436e8ed7d3da8ab8e6bb |
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| Source note | uspto-grants-2014_06 |
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