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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746054Generated: November 3, 2026

Hydrochloric Acid → 2,2-Difluoro-5-iodo-6-methoxybenzo[d][1,3]dioxole

https://huagongshe.com/reaction/1746054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium IodideHCID 5238—
ReactantSodium BisulfiteHCID 23665763—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 90413709HCID 90413709—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2,2-Difluoro-5-iodo-6-methoxybenzo[d][1,3]dioxoleHCID 9041497183.1%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

2,2-Difluoro-6-methoxybenzo[d][1,3]dioxol-5-amine (1.4 g, 6.9 mmol) was dissolved in dichloromethane (5 mL) and added in portions to rapidly stirred concentrated HCl (75 mL) to form a loose white slurry. The mixture was cooled to 0-5° C. and treated in portions with sodium nitrite (710 mg, 10 mmol) in water (10 mL). After 40 min, this mixture was poured as a thin stream into a solution of sodium iodide (3.1 g, 21 mmol) in water (75 mL) rapidly stirred with dichloromethane (50 mL). After 45 min, the mixture was stirred with 15% NaHSO3 solution (20 mL) for 10 min. The separated aqueous phase was extracted with dichloromethane (30 mL), and the combined extracts were washed with saturated NaCl (15 mL), dried (Na2SO4) and evaporated. The material was purified by chromatography on silica with a 0-15% ethyl acetate-hexane gradient to afford the title compound as a white solid (1.8 g, 83%): mp 50-51° C.; 1H NMR (400 MHz, CDCl3) δ 7.45 (s, 1H), 6.69 (s, 1H), 3.86 (s, 3H); 19F NMR (376 MHz, CDCl3) δ −49.81 (s); EIMS m/z 314.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149038B2
Source datasetuspto-grants-2015_10
ORD IDord-76285d428cc7422095b3ae0c3f61b9f9
Source noteuspto-grants-2015_10