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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241117Generated: November 4, 2026

Ammonium Chloride → HCID 59306518, compound

https://huagongshe.com/reaction/2241117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantCornforth reagentHCID 2724130—
ReactantHCID 23131134HCID 23131134—
ReactantEthanol sodium ethoxideHCID 23706232—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 59306518HCID 5930651891%

Reaction Steps

Ethyl 3-acetoxymethyl-2,4,5-trifluorobenzoate (15.0 g, 54.2 mmol) was dissolved in ethanol (280 mL), and to the resultant solution, 21 wt % sodium ethoxide-ethanol solution (18.9 mL, 54.2 mmol) was added dropwise while cooling with ice. The resultant mixture was stirred at the same temperature for 10 minutes. While cooling with ice, saturated aqueous ammonium chloride (300 mL) was added to the reaction mixture and ethanol was concentrated under reduced pressure. The residual aqueous layer was extracted with ethyl acetate (300 mL×2). The organic layers were combined and washed with saturated brine (500 mL), followed by drying with sodium sulfate anhydrate. After filtration, the filtrate was concentrated under reduced pressure. The residue was dissolved in dichloromethane (50 mL), and while cooling with ice, the resultant solution was added dropwise to a suspension prepared through adding pyridinium dichromate (PDC) (40.2 g, 107 mmol) and Molecular Sieves 4A (40 g) to dichloromethane (150 mL). After completion of dropwise addition, the reaction mixture was stirred at room temperature for 16 hours, and diethyl ether (200 mL) and silica gel (40 g) were added thereto. The resultant mixture was concentrated under reduced pressure until the volume of the solvent was reduced to half. The solid matter that precipitated was separated through filtration and washed with diethyl ether. Subsequently, the filtrate and the wash solution were combined. The mixture was concentrated under reduced pressure. The residue was dissolved in ethanol (200 mL). Hydroxylamine hydrochloride (3.90 g, 56.1 mmol) was added to the resultant solution, and the mixture was stirred at 50° C. for 19 hours. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in ethyl acetate (300 mL). The resultant solution was washed with water (300 mL) and saturated brine (300 mL), and dried with sodium sulfate anhydrate. After filtration, the filtrate was concentrated under reduced pressure. The residue was recrystallized from chloroform/n-hexane, to thereby yield the title compound as a white solid (12.2 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723524B2
Source datasetuspto-grants-2010_05
ORD IDord-076f24bbe04b4527ac0e864fc527140d
Source noteuspto-grants-2010_05