Reaktion #1564463

Reaktionsgleichung

Sodium hydride

6-hydroxycoumarin

geranylgeranyl bromide

→

desired compound

6-(((2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl)oxy)-2H-chromen-2-one

Lösungsmittel

DMF

DMF

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeAn oven-dried 50 mL round bottom flask was prepared with a magnetic stirring bar
2. 2
   workup.STIRRINGthe solution was stirred at 0° C. for 30 minutes
3. 3
   Temperaturcooled to 0° C.
4. 4
   workup.ADDITIONadded drop-wise to the flask through the rubber septum
5. 5
   workup.WAITThe reaction mixture was left
6. 6
   workup.STIRRINGstirring under nitrogen at room temperature for 14 hours

Vorschrift

An oven-dried 50 mL round bottom flask was prepared with a magnetic stirring bar, a rubber septum cover, and a nitrogen inlet. 6-hydroxycoumarin (1) (474 mg, 2.92 mmol) and 4 mL of anhydrous DMF were added to the round bottom flask. The solution was stirred and cooled to 0° C. in a salt-ice bath. Sodium hydride (117 mg of 60% mineral oil suspension, 2.93 mmol) was added and the solution was stirred at 0° C. for 30 minutes. The crude geranylgeranyl bromide (302.85 mg) from the previous step was dissolved in anhydrous DMF, cooled to 0° C. and added drop-wise to the flask through the rubber septum using a syringe. The reaction mixture was left stirring under nitrogen at room temperature for 14 hours. The desired compound was isolated via preparative thin layer chromatography using a 7:3 Hexanes:Ethyl acetate solvent system. The purified product was characterized by 1H-NMR spectroscopy and high-resolution mass spectrometry (HRMS). 1H-NMR (300 MHz, CD3COCD3): δ 1.54-1.75 (15H), 1.93 (m, 12H), 4.65 (2H), 5.09 (3H), 5.53 (1H), 6.40 (1H), 7.11 (3H), 7.81 (1H). HRMS (EI) Calcd. for C79H38O3: 434.28210. found: 434.28236.

Quelle