Ethyl 4-[[3,5-bis(trimethylsilyl)benzoyl]amino]-2-fluorocinnamate → (E)-Ethyl 3-[4-[[3,5-bis(trimethylsilyl)benzoyl]amino]-2,5-difluorophenyl]-2-butenoate

HRID 2265097

Reaktionsgleichung

Reaktionsgleichung von HRID 2265097
[NH2:1][C:2]1[C:7]([F:8])=[CH:6][C:5](/[C:9](/[CH3:16])=[CH:10]/[C:11]([O:13][CH2:14][CH3:15])=[O:12])=[C:4]([F:17])[CH:3]=1.[CH3:18][Si:19]([CH3:48])([CH3:47])[C:20]1[CH:21]=[C:22]([CH:40]=[C:41]([Si:43]([CH3:46])([CH3:45])[CH3:44])[CH:42]=1)[C:23](NC1C=CC(C=CC(OCC)=O)=C(F)C=1)=[O:24]>>[CH3:44][Si:43]([CH3:46])([CH3:45])[C:41]1[CH:40]=[C:22]([CH:21]=[C:20]([Si:19]([CH3:48])([CH3:47])[CH3:18])[CH:42]=1)[C:23]([NH:1][C:2]1[C:7]([F:8])=[CH:6][C:5](/[C:9](/[CH3:16])=[CH:10]/[C:11]([O:13][CH2:14][CH3:15])=[O:12])=[C:4]([F:17])[CH:3]=1)=[O:24]

Komponenten

3

Versuchsvorschrift

BTMB (800 mg) and Compound 10a (869 mg) were reacted in the same manner as Compound 2b was synthesized. After the reaction was over, the reaction mixture was separated with ethyl acetate and water. The organic layer was washed once with water and once with a saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by column chromatography (5% ethyl acetate/n-hexane) to obtain Compound 10b (674 mg, 46%) as a light yellow solid.

Aufarbeitung

  1. customwas synthesized
  2. customwas separated with ethyl acetate and water
  3. washThe organic layer was washed once with water and once with a saturated sodium chloride solution
  4. dry with materialdried over anhydrous sodium sulfate
  5. distillationThe solvent was distilled off
  6. customthe residue was purified by column chromatography (5% ethyl acetate/n-hexane)

Quellen und Nachweise

ORD-Eintrag
ord-8891bfeb29be478581e150da1efe3786
Quelldatensatz
uspto-grants-2010_12
Patentnummer
US07855300B2

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