Sodium Carbonate → 3-Iodo-4-(2-(thiophen-3-yl)ethoxy)pyridine 1-oxide

HRID 84595

Reaktionsgleichung

Reaktionsgleichung von HRID 84595
ClC1C=CC=C(C(OO)=[O:9])C=1.[I:12][C:13]1[CH:14]=[N:15][CH:16]=[CH:17][C:18]=1[O:19][CH2:20][CH2:21][C:22]1[CH:26]=[CH:25][S:24][CH:23]=1.C(=O)([O-])[O-].[Na+].[Na+]>C(Cl)Cl>[I:12][C:13]1[CH:14]=[N+:15]([O-:9])[CH:16]=[CH:17][C:18]=1[O:19][CH2:20][CH2:21][C:22]1[CH:26]=[CH:25][S:24][CH:23]=1

Komponenten

5

Edukt 3

HCID 10340Sodium CarbonateHCID 70297m-Chloroperbenzoic acidHCID 579002113-Iodo-4-(2-(thiophen-3-yl)ethoxy)pyridine

Produkt 1

HCID 582840413-Iodo-4-(2-(thiophen-3-yl)ethoxy)pyridine 1-oxideAusbeute 96,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

m-Chloroperbenzoic acid (1.55 g, 6.29 mmol) was added portionwise to a solution of 1.0 g (3.02 mmol) of 3-iodo-4-(2-(thiophen-3-yl)ethoxy)pyridine in 150 ml of methylene chloride. The mixture was stirred for 18 hours then mixed with 100 ml of 1 M aqueous sodium carbonate. The organic layer was separated and the aqueous one was extracted 2 times with 10 ml of methylene chloride. Combined organic extracts were washed with brine and dried over sodium sulfate. The solution was concentrated in vacuum to give 3-iodo-4-(2-(thiophen-3-yl)ethoxy)pyridine 1-oxide (1.01 g, 92%). MS: (ESI+) 348.0

Aufarbeitung

  1. customThe organic layer was separated
  2. extractionthe aqueous one was extracted 2 times with 10 ml of methylene chloride
  3. washCombined organic extracts were washed with brine
  4. dry with materialdried over sodium sulfate
  5. concentrationThe solution was concentrated in vacuum

Quellen und Nachweise

ORD-Eintrag
ord-ea2c75500cfb4e2780ca451f59757856
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08846762B2

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