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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452366Generated: October 26, 2026

Water → Tolpyralate

https://huagongshe.com/reaction/452366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Chloroethyl methyl carbonateHCID 13506641—
ReactantHCID 178463133HCID 178463133—
CatalystTetrabutylammonium BromideHCID 74236—
SolventMethyl Ethyl KetoneHCID 6569—
ProductTolpyralateHCID 4447318247.4%

Reaction Steps

5-Hydroxy-1-ethylpyrazol-4-yl 3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)phenyl ketone (300 mg) was dissolved in 2-butanone (10 mL), and potassium carbonate (130 mg) and tetrabutylammonium bromide (15 mg) were added. After stirring at room temperature for 10 minutes, 1-chloroethyl methyl carbonate (purity: 85%, 270 mg) was added at room temperature, followed by heating and refluxing for 3 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and poured into water and then extracted with ethyl acetate. The organic layer was washed with 1N hydrochloric acid and a saturated sodium chloride aqueous solution, followed by drying over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The obtained residue was purified by column chromatography with n-hexane:ethyl acetate=1:1, to obtain the desired product (180 mg) as slightly yellow solid. The NMR spectrum data of this product are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492310B2
Source datasetuspto-grants-2013_07
ORD IDord-9b6fd4b205ac4a88ba051d9c4f4791d4
Source noteuspto-grants-2013_07