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

HRID 1746054
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1746054
[F:1][C:2]1([F:14])[O:6][C:5]2[CH:7]=[C:8]([O:12][CH3:13])[C:9](N)=[CH:10][C:4]=2[O:3]1.Cl.N([O-])=O.[Na+].[I-:20].[Na+].OS([O-])=O.[Na+]>ClCCl.O>[F:1][C:2]1([F:14])[O:6][C:5]2[CH:7]=[C:8]([O:12][CH3:13])[C:9]([I:20])=[CH:10][C:4]=2[O:3]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

HCID 313Hydrochloric AcidHCID 5238Sodium IodideHCID 23665763Sodium BisulfiteHCID 23668193Sodium NitriteHCID 90413709HCID 90413709, Verbindung

Produkt 1

HCID 904149712,2-Difluoro-5-iodo-6-methoxybenzo[d][1,3]dioxoleAusbeute 83,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel2×HCID 6344DichloromethaneLösungsmittel2×

Reaktionsbedingungen

Temperatur
2.5 °C

Versuchsvorschrift

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.

Aufarbeitung

  1. additionadded in portions
  2. customto form a loose white slurry
  3. waitAfter 45 min
  4. extractionThe separated aqueous phase was extracted with dichloromethane (30 mL)
  5. washthe combined extracts were washed with saturated NaCl (15 mL)
  6. dry with materialdried (Na2SO4)
  7. customevaporated
  8. customThe material was purified by chromatography on silica with a 0-15% ethyl acetate-hexane gradient

Quellen und Nachweise

ORD-Eintrag
ord-76285d428cc7422095b3ae0c3f61b9f9
Quelldatensatz
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09149038B2

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