Diethyl Ether → 2-methoxy-10H-phenothiazine-1-carbaldehyde

HRID 393520

Reaktionsgleichung

Reaktionsgleichung von HRID 393520
[CH3:1][O:2][C:3]1[CH:16]=[CH:15][C:14]2[S:13][C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[NH:6][C:5]=2[CH:4]=1.[CH2:17]([O:19]CC)C.[Li]CCCC.CN(C=O)C>CCCCCC.O>[CH3:1][O:2][C:3]1[CH:16]=[CH:15][C:14]2[S:13][C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[NH:6][C:5]=2[C:4]=1[CH:17]=[O:19]

Komponenten

7

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

4.6 g (20 mmol) of 2-methoxy-10H-phenothiazine are dissolved, under an argon atmosphere, in a three-necked flask, containing 140 ml anhydrous ethyl ether. 20 ml (50 mmol) of a solution of nBuLi (2.5 M) in hexane is then added dropwise, at 20° C. The reaction mixture is agitated for 3 hours at 20° C. before the dropwise addition of 6.2 ml (80 mmol) of anhydrous DMF. Agitation is maintained for another 15 hours at 20° C. The whole is then poured into 150 ml ice-cooled water and the product is extracted twice using 200 ml of ethyl acetate. The organic solution is washed with 100 ml of salt water, dried over MgSO4, filtered and concentrated under vacuum. The evaporation residue is taken up in diisopropyl ether, filtered and dried to produce a red solid with a yield of 30%. Melting point: 155-160° C.

Aufarbeitung

  1. extractionthe product is extracted twice
  2. washThe organic solution is washed with 100 ml of salt water
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated under vacuum
  6. filtrationfiltered
  7. customdried
  8. customto produce a red solid with a yield of 30%

Quellen und Nachweise

ORD-Eintrag
ord-27b44ed0476c4c9bb0dc456a9c67c7b7
Quelldatensatz
uspto-grants-2004_10
Patentnummer
US06809090B2

Verknüpfte Notizen

Wird geladen…