Reaktion #1880960

ord-7c04250c87944dd8b5249da28c9d67db

Reaktionsgleichung

O
water
C[Si](C)(C)I
iodotrimethylsilane
COc1cc2c(cc1OC)C(C)CC2
5,6-dimethoxy-1-methylindane
C[Si](C)(C)I
iodotrimethylsilane
CC1CCc2cc(O)c(O)cc21
1-methylindane-5,6-diol
Ausbeute 93.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe product was extracted twice
  2. 2
    WaschenThe combined extracts were washed with 100 ml of 40% sodium hydrogen sulfite solution, 100 ml of water and 50 ml of saturated sodium chloride solution
  3. 3
    Trocknendried over sodium sulfate
  4. 4
    Einengenconcentrated on a rotary evaporator

Vorschrift

Over 90 min at room temperature, 27.5 ml (202 mmol) of iodotrimethylsilane were added dropwise with stirring to a solution of 19.4 g (101 mmol) of 5,6-dimethoxy-1-methylindane in 150 ml of acetonitrile. The mixture was stirred for a further 2.5 d at room temperature, in the course of which, after 48 h, again 10 ml (73.5 mmol) of iodotrimethylsilane were added. The reaction mixture was then poured into 500 ml of water and the product was extracted twice, each time with 200 ml of ether. The combined extracts were washed with 100 ml of 40% sodium hydrogen sulfite solution, 100 ml of water and 50 ml of saturated sodium chloride solution, dried over sodium sulfate and concentrated on a rotary evaporator. After flash chromatography (pentane/ether, 2:1, Rf=0.28) on silica gel, 15.5 g (93%) of 1-methylindane-5,6-diol were obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07022664B2uspto-grants-2006_04