Reaktion #306006

Reaktionsgleichung

2-isopropoxy-3-methoxy-5-iodophenol

1-(tert-butyldimethylsilyl) -3-(tert-butyldimethylsilyloxy)propyne

lithium chloride

sodium carbonate

→

title compound

Ausbeute 96.0%

2-t-Butyldimethylsilyl-3-(t-butyldimethylsilyloxymethylene)-6-methoxy-7-isopropoxybenzofuran

Ausbeute 96.0%

Lösungsmittel

dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigewas deoxygenated 4 times by evacuation and backfilling with nitrogen
2. 2
   Sonstigethe reaction vessel was degassed twice with nitrogen
3. 3
   Sonstigethe solvent was removed by distillation under vacuum
4. 4
   workup.DISSOLUTIONThe residue was dissolved in ethyl acetate (75 mL)
5. 5
   workup.STIRRINGstirred well
6. 6
   Filtrationfiltered
7. 7
   workup.ADDITIONtreated with triethylamine (5 mL)
8. 8
   EinengenThe solution was concentrated onto silica gel (10 g)
9. 9
   Sonstigepurified by flash chromatography (silica gel, eluent=hexane/diethyl ether/triethylamine; 95:5:1%)

Vorschrift

A suspension of 2-isopropoxy-3-methoxy-5-iodophenol (4.41 mmol), 1-(tert-butyldimethylsilyl) -3-(tert-butyldimethylsilyloxy)propyne (1.5 g, 5.28 mmol), lithium chloride (189 mg, 4.45 mmol) and sodium carbonate (2.34 g, 22.08 mmol) in dry dimethylformamide (5 mL) at 100° C. was deoxygenated 4 times by evacuation and backfilling with nitrogen. Palladium acetate (135 mg, 0.60 mmol) was added and the reaction vessel was degassed twice with nitrogen. The reaction mixture was then stirred at this temperature for 4 hours (tlc) and the solvent was removed by distillation under vacuum. The residue was dissolved in ethyl acetate (75 mL), stirred well, filtered and treated with triethylamine (5 mL). The solution was concentrated onto silica gel (10 g) and purified by flash chromatography (silica gel, eluent=hexane/diethyl ether/triethylamine; 95:5:1%) to afforded the title compound as a yellow oil (1.45 g, 96%); 1H NMR (300 MHz, CDCl3) δ 7.24(d, 1H, J=8.45 Hz), 6.88(d, 1H, J=8.47 Hz), 4.80(s, 2H, CH2), 4.73(m, 1H), 3.88(s, 3H, OMe), 1.36(d, 6H, J=6.17 Hz), 0.94(s, 9H), 0.92(s, 9H), 0.35(s, 6H), 0.12(s, 6H).

Quelle