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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591861Generated: November 1, 2026

1,4-Dioxane → HCID 26696954, compound

https://huagongshe.com/reaction/1591861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant4-Fluoro-3-nitroanilineHCID 67768—
Reactant2-Chloro-4-fluorobenzoyl chlorideHCID 2736546—
SolventEthyl AcetateHCID 8857—
ProductHCID 26696954HCID 2669695485%

Reaction Steps

Combine 4-fluoro-3-nitroaniline (1.0 g, 6.4 mmol) with dioxane (20 mL). Treat mixture with 2-chloro-4-fluorobenzoyl chloride (1.6 g, 8.3 mmol). Stir the reaction overnight at room temperature. Transfer the reaction mixture into ethyl acetate (220 mL), then wash successively with aqueous HCl (1N, 50 mL), aqueous NaOH (1N, 50 mL), saturated aqueous NaCl (50 mL). Dry the organic layer over anhydrous sodium sulfate, then evaporate the solvent under reduced pressure. Further purify the residue by chromatography on silica gel, using a gradient of 10–30% ethyl acetate in hexanes to obtain the title intermediate (1.7 g, 85% yield): mass spectrum (ion spray): m/z=313.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291632B2
Source datasetuspto-grants-2007_11
ORD IDord-9087b76bc4534c9da81985fc6ee60bb2
Source noteuspto-grants-2007_11