Reacción #1880960

ord-7c04250c87944dd8b5249da28c9d67db

Ecuación de reacción

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
Rendimiento 93.5%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónthe product was extracted twice
  2. 2
    LavadoThe 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
    Secadodried over sodium sulfate
  4. 4
    Concentraciónconcentrated on a rotary evaporator

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07022664B2uspto-grants-2006_04