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Methane, dichloromethoxy- → HCID 19047057, Verbindung

HRID 1780615
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1780615
[CH3:1][C:2]1([CH3:14])[CH2:6][C:5]2[C:7]([CH3:13])=[C:8]([CH3:12])[CH:9]=[C:10]([CH3:11])[C:4]=2[O:3]1.[CH3:15][O:16]C(Cl)Cl>ClCCl.[Cl-].[Ti+4].[Cl-].[Cl-].[Cl-]>[CH3:1][C:2]1([CH3:14])[CH2:6][C:5]2[C:7]([CH3:13])=[C:8]([CH3:12])[C:9]([CH:15]=[O:16])=[C:10]([CH3:11])[C:4]=2[O:3]1
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Komponenten

5

Edukt 2

HCID 21004Methane, dichloromethoxy-HCID 19047070HCID 19047070, Verbindung

Produkt 1

HCID 19047057HCID 19047057, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 160960Diamminetetrachlorotitanate(IV)KatalysatorHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of 34.5 g of the 2,3-dihydro-2,2,4,5,7-pentamethylbenzofuran in 200 ml of absolute dichloromethane was added 200 ml of titanium chloride (IV) and 18 ml of α,α-dichloromethyl methyl ether at 0° C. With stirring at room temperature for 45 minutes and refluxing for 15 minutes, the reaction mixture was quenched with 300 ml of water and the aqueous layer was extracted with dichloromethane. The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford a crude product. Final purification was carried by recrystallization to afford 37.2 g of 2,3-dihydro-2,2,4,5,7-pentamethyl-benzofuran-6-carboxaldehyde as a white solid.

Aufarbeitung

  1. temperaturerefluxing for 15 minutes
  2. customthe reaction mixture was quenched with 300 ml of water
  3. extractionthe aqueous layer was extracted with dichloromethane
  4. dry with materialThe combined organic extracts were dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customto afford a crude product
  8. customFinal purification
  9. customwas carried by recrystallization

Quellen und Nachweise

ORD-Eintrag
ord-28b53685327d4b428ca714f85bce3f76
Quelldatensatz
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05631208

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