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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404571Generated: October 30, 2026

Diethyl Ether → Diisopropyl Ether

https://huagongshe.com/reaction/2404571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 66842008HCID 66842008—
ProductDiisopropyl EtherHCID 7914—
ProductHCID 68482693HCID 68482693—

Reaction Steps

4.6 g of 1-(5-(2,2,2-trifluoroethylthio)-2-fluoro-4-methylphenyl)hydrazine was dissolved in 100 mL of diethyl ether, and 1.85 g of acetic anhydride was dropwise added under cooling with ice, followed by stirring at room temperature for one hour. The obtained crystals were collected by filtration and washed with a solution of hexane:diisopropyl ether=3:1 (mass ratio) to obtain 4.41 g of N′-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}acetohydrazide in the form of colorless crystals. Then, to 4.4 g of this hydrazide, 1.93 g of ethyl acetoacetate and 4.02 g of phosphorus tribromide were added, followed by stirring at 50° C. for 2 hours. Then, after stirring under cooling with ice for 10 minutes, ice was put, and the pH was adjusted to 5 with a 1N sodium hydroxide aqueous solution. Then, extraction with ethyl acetate was carried out, followed by washing with a saturated salt solution, the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure, and the obtained residue was purified by column chromatography (ethyl acetate:hexane=1:3) to obtain 2.03 g of 1-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}-3-hydroxy-5-methylpyrazole in the form of colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802713B2
Source datasetuspto-grants-2014_08
ORD IDord-8913ca882d964fe8a7ceec9a6ae3f260
Source noteuspto-grants-2014_08