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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409071Generated: October 29, 2026

Hydrochloric Acid → HCID 86714471, compound

https://huagongshe.com/reaction/409071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantUreaHCID 1176—
ReactantSodium IodideHCID 5238—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 63036034HCID 63036034—
SolventWaterHCID 962—
ProductHCID 86714471HCID 8671447179.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 250-mL 4-necked round-bottom flask, was placed 4-(2,3-difluorophenoxy)-aniline (8.84 g, 39.96 mmol, 1.00 equiv), hydrogen chloride (10.14 g, 100.01 mmol, 2.50 equiv), and water (20 mL). A solution of NaNO2 (3.04 g, 44.06 mmol, 1.10 equiv) in water (10 mL) was added dropwise with stirring in portions at 0° C. The mixture was stirred at 0° C. for half an hour. To this was added urea (1 g, 16.65 mmol). The mixture was stirred at 0° C. for 20 min and poured into the solution of NaI (18 g, 120.00 mmol, 3.00 equiv) in water (20 mL) at room temperature. The resulting solution was stirred at room temperature for 1 h and then extracted with ethyl acetate. The organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum to give 10.5 g (79%) of 1,2-difluoro-3-(4-iodophenoxy)benzene as brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759358B1
Source datasetuspto-grants-2014_06
ORD IDord-d7642ef502e847ab82a2dd821e303238
Source noteuspto-grants-2014_06