Hydrochloric Acid → 1-[3-(2-{[Tert-butyl(dimethyl)silyl]oxy}ethyl)phenyl]ethanone

HRID 1246545Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1246545
Br[C:2]1[CH:3]=[C:4]([CH2:8][CH2:9][O:10][Si:11]([C:14]([CH3:17])([CH3:16])[CH3:15])([CH3:13])[CH3:12])[CH:5]=[CH:6][CH:7]=1.[Li]CCCC.[CH3:23][C:24](N(C)C)=[O:25].Cl>O1CCCC1.CCCCCC.O>[Si:11]([O:10][CH2:9][CH2:8][C:4]1[CH:3]=[C:2]([C:24](=[O:25])[CH3:23])[CH:7]=[CH:6][CH:5]=1)([C:14]([CH3:17])([CH3:16])[CH3:15])([CH3:13])[CH3:12]

Komponenten

8

Edukt 4

HCID 313Hydrochloric AcidHCID 31374DimethylacetamideHCID 11515183(3-Bromophenethoxy)(tert-butyl)dimethylsilaneHCID 178418339Butyllithium

Produkt 1

HCID 692256631-[3-(2-{[Tert-butyl(dimethyl)silyl]oxy}ethyl)phenyl]ethanone

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 8028TetrahydrofuranLösungsmittelHCID 8058HexaneLösungsmittel

Versuchsvorschrift

To a solution of 1.6 g of [2-(3-bromophenyl)ethoxy](tert-butyl)dimethylsilane in tetrahydrofuran (20 ml) was added n-BuLi in hexane (1.57M, 3.88 ml) at −70° C., then the reaction mixture was stirred at same temperature for 30 min. To the solution was added dimethylacetamide (1.42 ml) drop wise at the same temperature. The mixture was stirred for another 1 hour. To the reaction mixture were added water and 8 ml of 1N HCl under ice-cooling. The mixture was stirred for 1 hour, then extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography with n-hexane and ethyl acetate (20/1–10/1) as an eluent to give 1-[3-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)phenyl]ethanone (350 mg) as colorless oil.

Aufarbeitung

  1. stirringThe mixture was stirred for another 1 hour
  2. temperaturecooling
  3. stirringThe mixture was stirred for 1 hour
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by silica gel column chromatography with n-hexane and ethyl acetate (20/1–10/1) as an eluent

Quellen und Nachweise

ORD-Eintrag
ord-7932c995cf9a41b9b52e44f59945cd43
Quelldatensatz
uspto-grants-2006_10
Patentnummer
US07125901B2

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