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Tetrahydrofuran → HCID 19096191, Verbindung

HRID 486687
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 486687
[CH3:1][C:2]([CH3:18])([CH3:17])[C:3]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]([F:15])([F:14])[F:13])=[CH:8][C:7]=1[CH3:16])=[O:4].O1CCCC1.C([Li])CCC.[CH3:29][N:30]=[CH:31][C:32]1[S:33][CH:34]=[CH:35][C:36]=1[CH3:37]>C1(C)C=CC=CC=1.O>[CH3:1][C:2]([CH3:18])([CH3:17])[C:3]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]([F:13])([F:14])[F:15])=[CH:8][C:7]=1[CH2:16][CH:31]([NH:30][CH3:29])[C:32]1[S:33][CH:34]=[CH:35][C:36]=1[CH3:37])=[O:4]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 8028Tetrahydrofuran2×HCID 22414475HCID 22414475, VerbindungHCID 856047263-Methyl-2-thiophenecarboxaldehyde methylimineHCID 178418339Butyllithium

Produkt 1

HCID 19096191HCID 19096191, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962
Water
Lösungsmittel
HCID 1140TolueneLösungsmittel

Versuchsvorschrift

To a chilled (10° C.) solution of 12.81 g of 2,2-dimethyl-N-(2-methyl-4-trifluoromethylphenyl)propanamide and 200 ml of anhydrous tetrahydrofuran, was added dropwise over 20 min, 48 ml of a 2.5M solution of n-butyllithium in hexanes, with stirring. The solution was stirred, with cooling, for 1 hr, and 10.65 g of an 85% solution of 3-methyl-2-thiophenecarboxaldehyde methylimine in toluene, and 20 ml of tetrahydrofuran was added, dropwise over 10 min, with stirring. After stirring and cooling for 1.5 hr, 60 ml of water was added, and the mixture was evaporated. The residue was diluted with water and extracted with dichloromethane. The combined, organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was separated by HPLC (Waters Associates Prep LC/System 500, silica gel, 200 ml/min flow rate; the residue was dissolved in sufficient ethyl acetate-hexane (1:1) to give 50 ml of solution, and the solution was applied in 25 ml portions to the columns, Gow Mac UV detector). The appropriate fractions were combined and concentrated. The residue was purified again by preparative HPLC under similar conditions, and finally, using a single recycle (elution with ethyl acetate-hexane (1:1)) to afford 9.53 g of product, mp 64°-69° C.

Aufarbeitung

  1. additionwas added dropwise over 20 min
  2. temperaturewith cooling, for 1 hr
  3. stirringwith stirring
  4. stirringAfter stirring
  5. temperaturecooling for 1.5 hr
  6. customthe mixture was evaporated
  7. additionThe residue was diluted with water
  8. extractionextracted with dichloromethane
  9. dry with materialorganic phase was dried over anhydrous sodium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated
  12. customThe residue was separated by HPLC (Waters Associates Prep LC/System 500, silica gel, 200 ml/min flow rate
  13. dissolutionthe residue was dissolved in sufficient ethyl acetate-hexane (1:1)

Quellen und Nachweise

ORD-Eintrag
ord-4e66fb4efce54cf9855e1f546deb9618
Quelldatensatz
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05292760

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