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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087897Generated: October 31, 2026

Ammonium Hydroxide → HCID 15058685, compound

https://huagongshe.com/reaction/1087897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 15058687HCID 15058687—
CatalystDimethylformamideHCID 6228—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 15058685HCID 15058685—

Reaction Steps

A mixture of 1.3 gram (0.0054 mole) of 2,3-di(2-fluoroethoxy)benzoic acid, 1.0 gram (0.0080 mole) of oxalyl chloride, and one drop of N,N-dimethylformamide in 20 ml of diethyl ether was stirred at room temperature for approximately 18 hours. The solvent was evaporated from the reaction mixture leaving a residue. This residue was dissolved in 100 ml of methylene chloride, and the resulting organic solution was added slowly to a stirred, cold (0° C.) aqueous solution of ammonium hydroxide (5 ml of 30% solution). This mixture was allowed to warm to room temperature and stir for approximately 18 hours. The mixture was washed with an aqueous, sodium bicarbonate solution followed by an aqueous, saturated sodium chloride solution. The washed organic phase was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure leaving a solid residue. Recrystallization of this solid from a mixture of toluene and n-hexane yielded 0.6 gram of 2,3-di(2-fluoroethoxy)benzamide, mp 100°-101° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04960884
Source datasetuspto-grants-1990_10
ORD IDord-55c65ef56b1147df9f8292a37d4086fe
Source noteuspto-grants-1990_10