StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

1,2-Dimethoxyethane → 3-Vinyl-6,7-dihydro-[1,4]dioxino[2,3-c]pyridazine

HRID 2233177
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2233177
Cl[C:2]1[N:7]=[N:6][C:5]2[O:8][CH2:9][CH2:10][O:11][C:4]=2[CH:3]=1.[CH2:12]([CH2:15]OC)OC>>[CH:12]([C:2]1[N:7]=[N:6][C:5]2[O:8][CH2:9][CH2:10][O:11][C:4]=2[CH:3]=1)=[CH2:15]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 80711,2-DimethoxyethaneHCID 552674403-Chloro-6,7-dihydro-[1,4]dioxino[2,3-c]pyridazine

Produkt 1

HCID 675264353-Vinyl-6,7-dihydro-[1,4]dioxino[2,3-c]pyridazineAusbeute 50 %

Reaktionsbedingungen

Temperatur
95 °C

Versuchsvorschrift

A solution of 3-chloro-6,7-dihydro[1,4]dioxino[2,3-c]pyridazine (13.6 g, 0.079 mol) containing ca. 15% of a bromo species in dimethoxyethane (400 ml) was degassed under argon for 10 min then tetrakis(triphenylphosphine)palladium (0) (2 g), potassium carbonate (10.33 g), triethenylboroxin pyridine complex (11.32 g) and water (55 ml) were added. The mixture was heated at 95° C. for 48 h and cooled and evaporated to dryness. The mixture was treated with aqueous sodium bicarbonate solution and extracted (5×) with DCM. Extracts were dried (sodium sulphate), evaporated and the residue chromatographed on silica gel (500 g), eluting with 0-100% ethyl acetate-hexane, affording the product (6.43 g, 50%); [also some impure fractions (1.8 g)]

Aufarbeitung

  1. customwas degassed under argon for 10 min
  2. additiontetrakis(triphenylphosphine)palladium (0) (2 g), potassium carbonate (10.33 g), triethenylboroxin pyridine complex (11.32 g) and water (55 ml) were added
  3. temperaturecooled
  4. customevaporated to dryness
  5. additionThe mixture was treated with aqueous sodium bicarbonate solution
  6. extractionextracted (5×) with DCM
  7. dry with materialExtracts were dried (sodium sulphate)
  8. customevaporated
  9. customthe residue chromatographed on silica gel (500 g)
  10. washeluting with 0-100% ethyl acetate-hexane

Quellen und Nachweise

ORD-Eintrag
ord-bca3196f050e4950948142be4beab999
Quelldatensatz
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07709483B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion