Triethylsilane → N-[4-(2-Bromoethyl)-2,5-dimethylphenyl]acetamide
Reaktionsgleichung
C([SiH](CC)CC)C.[Br:8][CH2:9][C:10]([C:12]1[C:17]([CH3:18])=[CH:16][C:15]([NH:19][C:20](=[O:22])[CH3:21])=[C:14]([CH3:23])[CH:13]=1)=O>FC(F)(F)C(O)=O>[Br:8][CH2:9][CH2:10][C:12]1[C:17]([CH3:18])=[CH:16][C:15]([NH:19][C:20](=[O:22])[CH3:21])=[C:14]([CH3:23])[CH:13]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Triethylsilane 60 mL (375 mmol) was added to trifluoroacetic acid 360 mL and stirred until a homogenous mixture was obtained (15 minutes). This mixture was then added to solid N-[4-(2-bromo-acetyl)-2,5-dimethyl-phenyl]-acetamide 28.88 g (101.64 mmol) in an ice-cooled flask. The flask was capped with a Dryerite-filled tube (as a gas outlet) and the mixture was stirred on ice bath for 1 hour, then at room temperature for 1 day. The reaction mixture was evaporated and the obtained thick residue was suspended in hexane (0.3 L). Water (100 mL) was added and the mixture was stirred and occasionally shaken for about 1 hour. The formed precipitate was collected by filtration, washed repeatedly with plenty of hexane and water, compressed on the frit, dried by air suction, then on high vacuum.