Dichloromethane → 4-bromo-2-(cyclohexylmethyl)-3,5,6,7-tetrahydro-s-indacen-1(2H)-one

HRID 538859Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 538859
[Al+3].[Cl-].[Cl-].[Cl-].ClCCl.[CH:8]1([CH2:14][CH:15]2[CH2:26][C:25]3[C:17](=[CH:18][C:19]4[CH2:20][CH2:21][CH2:22][C:23]=4[CH:24]=3)[C:16]2=[O:27])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1.[Br:28]Br>>[CH:8]1([CH2:14][CH:15]2[CH2:26][C:25]3[C:17](=[CH:18][C:19]4[CH2:20][CH2:21][CH2:22][C:23]=4[C:24]=3[Br:28])[C:16]2=[O:27])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1

Komponenten

5

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a mixture of 40.9 g (0.305 mol) of AlCl3 in 180 ml of dichloromethane 32.7 g (0.122 mol) of 2-(cyclohexylmethyl)-3,5,6,7-tetrahydro-s-indacen-1(2H)-one was added. To this mixture cooled to 0° C. 21.5 g (0.134 mol) of bromine was added dropwise by vigorous stirring for 45 min at 0-5° C. The resulting mixture was stirred for 12 h at ambient temperature and then poured on 1000 cm3 of ice. The organic layer was separated, and the aqueous layer was extracted with 3×200 ml of dichloromethane. The combined organic extract was dried over Na2SO4 and then evaporated to dryness. This product was further used without an additional purification. Yield 39.5 g (93%).

Aufarbeitung

  1. additionwas added
  2. stirringThe resulting mixture was stirred for 12 h at ambient temperature
  3. customThe organic layer was separated
  4. extractionthe aqueous layer was extracted with 3×200 ml of dichloromethane
  5. extractionThe combined organic extract
  6. dry with materialwas dried over Na2SO4
  7. customevaporated to dryness
  8. customThis product was further used without an additional purification

Quellen und Nachweise

ORD-Eintrag
ord-fcf1d55813314427b0c2d3d5ca4f02e3
Quelldatensatz
uspto-grants-2014_10
Patentnummer
US08865848B2

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