5-Bromo-1-indanone → (E)-5-bromo-1-(methoxymethylene)-2,3-dihydro-1H-indene

HRID 1886807

Reaktionsgleichung

Reaktionsgleichung von HRID 1886807
[Cl-].[CH3:2][O:3][CH2:4][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.CC(C)([O-])C.[K+].[Br:30][C:31]1[CH:32]=[C:33]2[C:37](=[CH:38][CH:39]=1)[C:36](=O)[CH2:35][CH2:34]2>C1COCC1>[Br:30][C:31]1[CH:32]=[C:33]2[C:37](=[CH:38][CH:39]=1)/[C:36](=[CH:2]/[O:3][CH3:4])/[CH2:35][CH2:34]2

Komponenten

5

Reaktionsbedingungen

Temperatur
-20 °C

Versuchsvorschrift

To a suspension of (methoxymethyl)triphenylphosphonium chloride (39.7 g, 116 mmol) in THF (210 ml) at −20° C. was added dropwise 1M potassium t-butoxide (95 ml, 95 mmol) and the solution stirred at −20° C. for 20 min. To this solution was added dropwise a solution of 5-bromo-2,3-dihydro-1H-inden-1-one (10.0 g, 47.4 mmol) in THF (230 ml) and stirring was continued at −20° C. for 30 min then warmed to room temperature and stirred for 2 h. The solution was filtered through Celite and the filtrate was concentrated in vacuo to give crude product which was purified by chromatography on a silica gel cartridge eluting with CH2Cl2/hexane to give the title compound (10.56 g, 93%).

Aufarbeitung

  1. stirringstirring
  2. waitwas continued at −20° C. for 30 min
  3. temperaturethen warmed to room temperature
  4. stirringstirred for 2 h
  5. filtrationThe solution was filtered through Celite
  6. concentrationthe filtrate was concentrated in vacuo
  7. customto give crude product which
  8. customwas purified by chromatography on a silica gel cartridge
  9. washeluting with CH2Cl2/hexane

Quellen und Nachweise

ORD-Eintrag
ord-73270432a9f84a9abc13314945bfb2e4
Quelldatensatz
uspto-grants-2013_08
Patentnummer
US08501238B2

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