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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260962Generated: October 30, 2026

Isoamyl Alcohol → HCID 57117418, compound

https://huagongshe.com/reaction/260962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl AlcoholHCID 31260—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 19436753HCID 19436753—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 57117418HCID 5711741895%

Reaction Steps

To a solution of 1.9 g (5.0 mmole) of 2-(2-chloro-5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluorophenoxy)-propanoic acid in 50 mL methylene chloride was added 1.3 mL (15.0 mmole) oxalyl chloride over 5 minutes, causing the evolution of gas. When this evolution ceased, one drop of DMF was added and the solution stirred until the gas evolution ceased. The solution was stripped to dryness in vacuo. The acid chloride was dissolved in 40 mL of 3-methyl-1-butanol and heated to reflux for one hour. The reaction mixture was cooled, diluted with 100 mL cold water and extracted with ethyl acetate. The ethyl acetate was washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified chromatographically using 25% ethyl acetate in hexane as the eluent to give 2.17 g (95%) of 2-(2-chloro-5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluorophenoxy)-propanoic acid, 3-methylbutyl ester as a white solid; mp 128° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05530126
Source datasetuspto-grants-1996_06
ORD IDord-a2c070b0110a4a3da64f0f03d65a5dbf
Source noteuspto-grants-1996_06