HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058111Generated: October 25, 2026
Water → 2-Oxo-2-pyridin-3-ylethyl 2,2-dimethylpropanoate
https://huagongshe.com/reaction/1058111
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pivalic acid | HCID 6417 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Chloro-1-(pyridin-3-yl)ethan-1-one--hydrogen chloride (1/1) | HCID 11665552 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Oxo-2-pyridin-3-ylethyl 2,2-dimethylpropanoate | HCID 15512452 | 92.1% |
Reaction Steps
Pivalic acid (5.3 g, 52 mmol), 8.8 g (104 mmol) of sodium hydrogen carbonate and 0.84 g (2.6 mmol) of tetrabutylammonium bromide were added to a solution of 5.0 g (26 mmol) of 3- (2-chloroacetyl) pyridine hydrochloride in 80 ml of THF at room temperature, and the mixture was refluxed for 2 hours. Water (100 ml) was added to the reaction mixture and the resulting mixture was extracted three times with 100 ml of ethyl acetate. The organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and then dried over sodium sulfate. The solvent was distilled off under reduced pressure and the product was isolated and purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give 5.3 g (yield 92%) of the desired 2-oxo-2-pyridin-3-ylethyl 2,2-dimethylpropanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06515134B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-2d3b44607df94cfbbe80004652460851 |
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| Source note | uspto-grants-2003_02 |
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