Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508333Generated: November 1, 2026

Hydrochloric Acid → HCID 71254993, compound

https://huagongshe.com/reaction/1508333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Chloro-2,4-pentanedioneHCID 74328—
Reactant3-Chloro-2-fluoroanilineHCID 75014—
ReactantSodium AcetateHCID 517045—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 89405943HCID 89405943—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 71254993HCID 71254993—

Reaction Conditions

Temperature0 °C

Reaction Steps

(E)-N′-(3-Chloro-2-fluorophenyl)-2-oxopropanehydrazonoyl chloride: To a solution of 3-chloro-2-fluoroaniline (1.511 mL, 13.74 mmol) in HCl (116 mL, 116 mmol) at 0° C. was added a solution of sodium nitrite (1.896 g, 27.5 mmol) in water (12 mL) dropwise while maintaining the temperature at 0° C. After completion of addition, the reaction was stirred at the same temperature for additional 30 mins. The pH of the reaction mixture was adjusted to 4.5 using solid sodium acetate. The resultant mixture was then treated dropwise with 3-chloropentane-2,4-dione (2.129 mL, 17.86 mmol) in methanol (12 mL). After completion of addition, the reaction mixture was allowed to warm to room temperature and stirred at room temperature overnight. The reaction mixture was diluted with water and then extracted with ether. The crude product was then purified by silica gel chromatography to isolate the desired product. MS(ESI) m/z: 249.0 (M+2H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221818B2
Source datasetuspto-grants-2015_12
ORD IDord-ff8e9a16ad8246d9b73139dc5abd771e
Source noteuspto-grants-2015_12