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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276115Generated: October 30, 2026

Triethylamine → HCID 178481846, compound

https://huagongshe.com/reaction/1276115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-3-(4,5-dihydroisoxazol-3-yl)-4-methylsulfonylbenzoyl chlorideHCID 11381666—
ReactantHCID 178481816HCID 178481816—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178481846HCID 17848184692.5%

Reaction Steps

At room temperature and under an atmosphere of protective gas, 43.60 g (0.13 mol) of 2-chloro-3-(4,5-dihydroisoxazol-3-yl)-4-methylsulfonylbenzoyl chloride in 375 ml of anhydrous dioxane and 13.56 g (0.134 mol) of triethylamine in 375 ml of anhydrous dioxane were simultaneously added dropwise to a solution of 12.74 g (0.13 mol) of 5-hydroxy-1-methylpyrazole and 300 ml of anhydrous dioxane. The reaction mixture was stirred at room temperature for 2 hours and then filtered off through silica gel, which was rinsed with dioxane. The eluate was concentrated under reduced pressure to about 500 ml and admixed with 17.94 g (0.13 mol) of dried, finely powdered potassium carbonate. After 6 hours under reflux, the solvent was distilled off under reduced pressure and the residue was taken up in about 700 ml of water. Insoluble components were filtered off and the pH of the filtrate was adjusted to 2-3 by slowly adding 10% strength hydrochloric acid. The precipitate that formed was filtered off with suction. 46.16 g (92% of theory) of 4-[2-chloro-3-(4,5-dihydroisoxazol-3-yl)-4-methylsulfonylbenzoyl]-5-hydroxy-1-methyl-1H-pyrazole were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06165944
Source datasetuspto-grants-2000_12
ORD IDord-145ac9989c3a4fb0975d5da5527bb0b3
Source noteuspto-grants-2000_12