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Stannane, tributyl(1-ethoxyethenyl)- → Ethyl 5-chloro-6-(1-ethoxyvinyl)nicotinate

HRID 57450
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 57450
[Cl:1][C:2]1[C:3](Cl)=[N:4][CH:5]=[C:6]([CH:12]=1)[C:7]([O:9][CH2:10][CH3:11])=[O:8].C([Sn](CCCC)(CCCC)[C:19]([O:21][CH2:22][CH3:23])=[CH2:20])CCC>[Cl-].C([N+](CC)(CC)CC)C.CC#N.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[Cl:1][C:2]1[C:3]([C:19]([O:21][CH2:22][CH3:23])=[CH2:20])=[N:4][CH:5]=[C:6]([CH:12]=1)[C:7]([O:9][CH2:10][CH3:11])=[O:8]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 2

HCID 619414Stannane, tributyl(1-ethoxyethenyl)-HCID 16762519Ethyl 5,6-Dichloronicotinate

Produkt 1

HCID 86730204Ethyl 5-chloro-6-(1-ethoxyvinyl)nicotinate

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 5946Tetraethylammonium ChlorideKatalysatorHCID 178418476HCID 178418476, VerbindungKatalysator
HCID 6342
Acetonitrile
Lösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a suspension of ethyl 5,6-dichloronicotinate (5.26 g, 23.90 mmol) and tetraethylammonium-chloride (11.88 g, 71.7 mmol) in MeCN (50 mL) was added tributyl(1-ethoxyvinyl)stannane (9.50 g, 26.3 mmol) and PdCl2(PPh3)2 (0.671 g, 0.956 mmol). The reaction was sealed, heated at 80° C. for 5 hours. A dark color clear solution resulted. The reaction mixture was then cooled to 20° C., concentrated and diluted with EtOAc (200 mL), and washed with water (50 mL) and brine (50 mL). The organic was then dried (Na2SO4) and concentrated to give crude ethyl 5-chloro-6-(1-ethoxyvinyl)nicotinate. The residue was then dissolved in THF (100 mL) and HCl (20 mL, 3M in H2O) was added. The reaction mixture was stirred at 20° C. for 5 hours, and saturated NaHCO3 solution was added until pH=8. The mixture was then diluted with EtOAc (200 mL) and water (50 mL). The phases were separated and the aqueous layer was extracted with EtOAc (2×50 mL). The combined organics was washed with brine (20 mL), dried (Na2SO4) and concentrated to afford the desired product (3.56 g). LCMS m/z 228.5 (M+H)+, Rt 0.83 min.

Aufarbeitung

  1. customThe reaction was sealed
  2. customA dark color clear solution resulted
  3. temperatureThe reaction mixture was then cooled to 20° C.
  4. concentrationconcentrated
  5. additiondiluted with EtOAc (200 mL)
  6. washwashed with water (50 mL) and brine (50 mL)
  7. dry with materialThe organic was then dried (Na2SO4)
  8. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-9c4ee16e440945a6bfeb745f1ec38fef
Quelldatensatz
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09434719B2

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