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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870094Generated: November 1, 2026

1-(2-Hydroxyethyl)-2-pyrrolidinone → 2-(2-Pyrrolidon-1-yl)ethyl 5-(4-Chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-2,4-dichlorobenzoate

https://huagongshe.com/reaction/1870094

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Hydroxyethyl)-2-pyrrolidinoneHCID 76980—
Reactant5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-2,4-dichlorobenzoyl chlorideHCID 15346389—
SolventPyridineHCID 1049—
Product2-(2-Pyrrolidon-1-yl)ethyl 5-(4-Chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-2,4-dichlorobenzoateHCID 18695175—

Reaction Steps

A solution of 1 g (2.6 mmol) of 5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-2,4-dichlorobenzoyl chloride and 0.5 g (3.8 mmol) of 2-(2-pyrrolidon-1-yl)ethanol in 20 ml of pyridine was stirred for approximately 15 hours, whereupon the reaction mixture was concentrated. The residue was treated with 10 ml of water and 20 ml of ethyl acetate. The organic phase was then separated off, dried over magnesium sulfate and concentrated. The crude product was purified by column chromatography on silica gel (eluent: initially hexane/ethyl acetate=1:1, then ethyl acetate). Yield: 0.8 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096689
Source datasetuspto-grants-2000_08
ORD IDord-42f718896fd74ac390c311ec4eba0731
Source noteuspto-grants-2000_08