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

Ethyl bromodifluoroacetate → (4-Amino-3-methyl-5-nitro-phenyl)-difluoro-acetic acid ethyl ester

HRID 470372
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 470372
I[C:2]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[C:5]([NH2:6])=[C:4]([CH3:12])[CH:3]=1.[CH2:13]([O:15][C:16](=[O:21])[C:17](Br)([F:19])[F:18])[CH3:14]>CS(C)=O.[Cu]>[CH2:13]([O:15][C:16](=[O:21])[C:17]([C:2]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[C:5]([NH2:6])=[C:4]([CH3:12])[CH:3]=1)([F:19])[F:18])[CH3:14]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 69585Ethyl bromodifluoroacetateHCID 248996464-Iodo-2-methyl-6-nitroaniline

Produkt 1

HCID 59784320(4-Amino-3-methyl-5-nitro-phenyl)-difluoro-acetic acid ethyl esterAusbeute 65,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23978CopperKatalysatorHCID 679Dimethyl SulfoxideLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a solution of 4-iodo-2-methyl-6-nitroaniline (2.78 g, 10 mmol) and 2-bromo-2,2-difluoroacetic acid ethyl ester (2.03 g, 10 mmol) in anhydrous DMSO (20 mL) was added copper powder (1.28 g, 20 mmol). The mixture was purged with N2 and heated at 60° C. in a sealed vial for 14 h. After being cooled to the room temperature, the reaction mixture was poured into 20% aqueous NH4Cl solution (300 mL). The resulting mixture was basified to pH=8.5 with saturated aqueous Na2CO3 solution and was extracted with EtOAc (3×100 mL). The organic extract was washed with brine (2×30 mL), dried over Na2SO4 and concentrated. The residue was purified by chromatography (40:1 hexanes/EtOAc) to afford the title compound (1.79 g, 65%). 1H NMR (CDCl3) δ 1.36 (t, 3H), 2.30 (s, 3H), 4.36 (q, 2H), 6.41 (br s, 2H NH), 7.51 (s, 1H), 8.33 (s, 1H). ESI-MS m/z 275 (MH+), 255 (M-F)+, 297 (M+Na)+, 549 (2M+1)+ and 571 (2M+Na)+.

Aufarbeitung

  1. customThe mixture was purged with N2
  2. temperatureAfter being cooled to the room temperature
  3. additionthe reaction mixture was poured into 20% aqueous NH4Cl solution (300 mL)
  4. extractionwas extracted with EtOAc (3×100 mL)
  5. extractionThe organic extract
  6. washwas washed with brine (2×30 mL)
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated
  9. customThe residue was purified by chromatography (40:1 hexanes/EtOAc)

Quellen und Nachweise

ORD-Eintrag
ord-655116c904c34a70b1446d555263f423
Quelldatensatz
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08629147B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion