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

Hydrogen Bromide → Methyl 2-bromo-3-[3-fluoro-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]propionate

HRID 1584344
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1584344
N([O-])=O.[Na+].[F:5][C:6]1[CH:7]=[C:8]([CH:10]=[CH:11][C:12]=1[O:13][CH2:14][C:15]1[N:16]=[C:17]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[O:18][C:19]=1[CH3:20])N.[BrH:27].[C:28]([O:32][CH3:33])(=[O:31])[CH:29]=[CH2:30]>O.[Cu]=O.CO.CC(C)=O>[Br:27][CH:29]([CH2:30][C:8]1[CH:10]=[CH:11][C:12]([O:13][CH2:14][C:15]2[N:16]=[C:17]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[O:18][C:19]=2[CH3:20])=[C:6]([F:5])[CH:7]=1)[C:28]([O:32][CH3:33])=[O:31]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 4

HCID 260Hydrogen BromideHCID 7294Methyl AcrylateHCID 108594853-Fluoro-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)anilineHCID 23668193Sodium Nitrite

Produkt 1

HCID 10983188Methyl 2-bromo-3-[3-fluoro-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]propionateAusbeute 76,8 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 14829Copper oxideKatalysator
HCID 180AcetoneLösungsmittel
HCID 887MethanolLösungsmittel
HCID 962WaterLösungsmittel

Versuchsvorschrift

A solution of sodium nitrite (NaNO2) (3.1 g) in water (5 ml) was added dropwise, at temperature ranging from 0 to 5° C., to a mixture of 3-fluoro-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)aniline (12.3 g), aqueous HBr (47%, 28.4 g) and acetone (150 ml)-methanol (50 ml). The mixture was stirred for 25 minutes at the same temperature range, to which was added methyl acrylate (21.3 g). The mixture was heated at temperatures ranging from 30 to 35° C., to which was then added copper oxide (Cu2O) (0.05 g) at the same temperature range. The whole mixture was vigorously stirred. The reaction mixture was stirred for further 30 minutes, which was then concentrated under reduced pressure. To the concentrate was added aqueous ammonia, which was subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with water, which was then dried (MgSO4), followed by distilling off the solvent under reduced pressure. The residue was subjected to column chromatography on silica gel. From the fraction eluted with ethyl acetate-hexane (1:4), was obtained methyl 2-bromo-3-[3-fluoro-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]propionate (14.2 g) as an oily product.

Aufarbeitung

  1. temperatureThe mixture was heated at temperatures
  2. customranging from 30 to 35° C., to which
  3. stirringThe whole mixture was vigorously stirred
  4. stirringThe reaction mixture was stirred for further 30 minutes
  5. concentrationwhich was then concentrated under reduced pressure
  6. additionTo the concentrate was added aqueous ammonia, which
  7. extractionwas subjected to extraction with ethyl acetate
  8. washThe ethyl acetate layer was washed with water, which
  9. dry with materialwas then dried (MgSO4)
  10. distillationby distilling off the solvent under reduced pressure
  11. washFrom the fraction eluted with ethyl acetate-hexane (1:4)

Quellen und Nachweise

ORD-Eintrag
ord-9675195a8748402f8263bc6655c24c40
Quelldatensatz
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05932601

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion