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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 90413709 | HCID 90413709 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2-Difluoro-5-iodo-6-methoxybenzo[d][1,3]dioxole | HCID 90414971 | 83.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09149038B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-76285d428cc7422095b3ae0c3f61b9f9 |
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| Source note | uspto-grants-2015_10 |
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