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Trifluoroacetic acid → 4-Chloro-5-iodo-2-methoxypyridine

HRID 886103
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 886103
[Cl:1][C:2]1[C:7]([I:8])=[CH:6][N:5]=[C:4](N)[CH:3]=1.[C:10](O)(C(F)(F)F)=[O:11].N(OC(C)(C)C)=O>CO>[Cl:1][C:2]1[C:7]([I:8])=[CH:6][N:5]=[C:4]([O:11][CH3:10])[CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6422Trifluoroacetic acidHCID 10906Tert-Butyl nitriteHCID 219491214-Chloro-5-iodopyridin-2-amine

Produkt 1

HCID 582045954-Chloro-5-iodo-2-methoxypyridineAusbeute 92,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of 4-chloro-5-iodo-pyridin-2-ylamine (64.2 g, 0.25 mol) in methanol (1.1 L) and TFA (93.7 mL, 1.26 mol) was added tert-butyl nitrite (150 mL, 1.26 mol) so as to maintain temperature less than 3° C. The resultant mixture was stirred at RT for 1 h then allowed to warm to RT and stirred for 16 h. The reaction was quenched by the careful addition of water then concentrated in vacuo to ¼ volume. The resultant residue was treated with water (1 L) and the precipitate formed collected by filtration and dried in vacuo at 35° C. to give the title compound (62.3 g, 92%). Contains 16% impurity. 1H NMR 400 MHz (DMSO-d) δ: 8.56 (1H, s), 7.20 (1H, s), 3.86 (3H, s).

Aufarbeitung

  1. temperatureto maintain temperature less than 3° C
  2. customThe reaction was quenched by the careful addition of water
  3. concentrationthen concentrated in vacuo
  4. additionThe resultant residue was treated with water (1 L)
  5. customthe precipitate formed
  6. filtrationcollected by filtration
  7. customdried in vacuo at 35° C.

Quellen und Nachweise

ORD-Eintrag
ord-91559219f0d246528335565c256544e9
Quelldatensatz
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08242104B2

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