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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218463Generated: October 30, 2026

Diisopropylethylamine → HCID 10162188, compound

https://huagongshe.com/reaction/2218463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantEthanol, 2-(aminooxy)-HCID 3014186—
ReactantHCID 23516247HCID 23516247—
SolventDimethylformamideHCID 6228—
ProductHCID 10162188HCID 1016218890%

Reaction Steps

To a solution of 2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-benzoic acid pentafluorophenyl ester (10.0 g, 17.4 mmol) in anhydrous dimethylformamide (36 mL) was added 2-(aminooxy)-ethanol (1.6 g, 20.8 mmol) and N,N-diisopropylethylamine (6.0 mL, 34.8 mmol). The resultant solution was stirred at ambient temperature for 16 h. The reaction mixture was concentrated to 20% volume then diluted with ethyl acetate (360 mL). The resultant solution was washed with water (6×60 mL) and brine (2×60 mL). The organics were dried over anhydrous magnesium sulfate and concentrated under reduced pressure to afford a white solid that was purified on silica gel. Elution with ethyl acetate-methanol (9:1) afforded 2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-benzamide (7.31 g, 90%) as a white solid. Recrystallization from methanol afforded analytically pure material, identical in all respects to the material prepared by method A.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07411001B2
Source datasetuspto-grants-2008_08
ORD IDord-7f69dd37b1d047d1b17dbb81bfc4d937
Source noteuspto-grants-2008_08