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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580257Generated: October 31, 2026

Hydrochloric Acid → 1-(2-Fluoro-4-chloro-5-hydroxyphenyl)-3,4,5-trimethylpyrazole

https://huagongshe.com/reaction/580257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-(2-Fluoro-4-chloro-5-methylsulfonyloxyphenyl)-3,4,5-trimethylpyrazoleHCID 13798232—
SolventEthanolHCID 702—
Product1-(2-Fluoro-4-chloro-5-hydroxyphenyl)-3,4,5-trimethylpyrazoleHCID 1379823395%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 1-(2-fluoro-4-chloro-5-methylsulfonyloxyphenyl)- 3,4,5-trimethylpyrazole (33.3 g), 2N aqueous sodium hydroxide (100 ml) and ethanol (50 ml) was stirred at 40° C. for 30 minutes. After cooling, the reaction mixture was acidified with aqueous hydrochloric acid and then extracted wth toluene. The toluene layer thus obtained was washed with water and dried over anhydrous sodium sulfate. Removal of the solvent by distillation in vacuo gave the titled compound (24.2 g) as a pale yellow crystalline solid. Recrystallization of this solid from a mixture of n-hexane/ethyl acetate yielded a white crystalline solid. m.p. 158°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04752326
Source datasetuspto-grants-1988_06
ORD IDord-f5fb9f8a334f4c218a4fce06a16ca2ff
Source noteuspto-grants-1988_06