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Diethyl Ether → HCID 86706873, Verbindung

HRID 717894
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 717894
[Cl:1][C:2]1[CH:7]=[C:6](I)[CH:5]=[C:4]([C:9]([F:12])([F:11])[F:10])[N:3]=1.C([Mg]Cl)(C)C.C(OCC)C.[O:23]1[CH2:26][C:25](=[O:27])[CH2:24]1>O1CCCC1>[Cl:1][C:2]1[CH:7]=[C:6]([C:25]2([OH:27])[CH2:26][O:23][CH2:24]2)[CH:5]=[C:4]([C:9]([F:12])([F:11])[F:10])[N:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 3283Diethyl EtherHCID 108597852-Chloro-4-iodo-6-(trifluoromethyl)pyridineHCID 150242543-OxetanoneHCID 178418918HCID 178418918, Verbindung

Produkt 1

HCID 86706873HCID 86706873, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028
Tetrahydrofuran
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of 2-chloro-4-iodo-6-(trifluoromethyl)pyridine (1.00 g, 3.25 mmol, European Journal of Organic Chemistry, (18), 3793-3798, 2004) in tetrahydrofuran (20 mL) at 0° C. was added dropwise 2.0 M isopropylmagnesium chloride in diethyl ether (1.95 mL, 3.90 mmol, Aldrich). After stirring for 30 minutes at 0° C., a solution of oxetan-3-one (0.281 g, 3.90 mmol, Synthonix) in Tetrahydrofuran (5 mL) was added. After stirring for 1 hour, the reaction was quenched by the addition of water and ammonium chloride. The product was extracted with two portions of ethyl acetate. The combined organic extracts were dried over sodium sulfate, filtered and concentrated. Flash chromatography, eluting with a gradient from 0-40% EtOAc in hexanes on a 40 g silica gel cartridge afforded purified product (0.31 g, 38%). LCMS (M+H)+: 254.1.

Aufarbeitung

  1. stirringAfter stirring for 1 hour
  2. customthe reaction was quenched by the addition of water and ammonium chloride
  3. extractionThe product was extracted with two portions of ethyl acetate
  4. dry with materialThe combined organic extracts were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. washFlash chromatography, eluting with a gradient from 0-40% EtOAc in hexanes on a 40 g silica gel cartridge
  8. customafforded
  9. custompurified product (0.31 g, 38%)

Quellen und Nachweise

ORD-Eintrag
ord-3c25f68e0f804c6f81c5b123a29c367a
Quelldatensatz
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09193733B2

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