Sodium Carbonate → Ethyl 2-(5-methyl-2-benzofuranyl)benzoate

HRID 1492761Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1492761
C(=O)([O-])[O-].[Na+].[Na+].Br[C:8]1[C:12]2[CH:13]=[C:14]([CH2:17]N3C(C(NCC)=O)=C(Cl)N=C3CCCC)[CH:15]=[CH:16][C:11]=2[O:10][C:9]=1C1C=CC=CC=1C1N=NN(C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)N=1.Br[C:64]1[CH:74]=[CH:73][CH:72]=[CH:71][C:65]=1[C:66]([O:68][CH2:69][CH3:70])=[O:67]>COCCOC.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH3:17][C:14]1[CH:15]=[CH:16][C:11]2[O:10][C:9]([C:64]3[CH:74]=[CH:73][CH:72]=[CH:71][C:65]=3[C:66]([O:68][CH2:69][CH3:70])=[O:67])=[CH:8][C:12]=2[CH:13]=1

Komponenten

6

Versuchsvorschrift

Sodium carbonate (1N; 60 ml) was added to a mixture of Intermediate 1 (4.7 g), ethyl 2-bromobenzoate (5.89 g) and tetrakis- triphenylphosphine palladium (0) (0.88 g) in DME (100 ml). The mixture was heated at reflux for 18 h, cooled to room temperature and then concentrated in vacuo. The residue was extracted with ether (3×100 ml) and the combined extracts washed with brine (1×100 ml) and dried. The solvent was evaporated to give a brown oil (5 g) which was purified by column chromatography eluting with System A (1:20) to give the title compound as a pale yellow oil (2.89 g).

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 18 h
  3. concentrationconcentrated in vacuo
  4. extractionThe residue was extracted with ether (3×100 ml)
  5. washthe combined extracts washed with brine (1×100 ml)
  6. customdried
  7. customThe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-6a7887bcdc524a1d885e3ecd3d223d0c
Quelldatensatz
uspto-grants-1994_12
Patentnummer
US05374646

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