تفاعل #710497
ord-f2f344c87c9d4a30a72092f6ede91c52
معادلة التفاعل
EtOAc
Trimethylsilylcyanid
4-chloro-5-(chloromethyl)-2-(trifluoromethyl)pyridine
Tetra-n-butylammoniumfluoride
→
[4-chloro-6-(trifluoromethyl)pyridin-3-yl]acetonitrile
المردود 65.1%
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
درجة الحرارة
25°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىwas consumed
- 2تركيزThe mixture was concentrated
- 3أخرىthe residue was purified by silica gel chromatography
- 4غسيلeluted with petroleum ether
الإجراء التجريبي
Trimethylsilylcyanid (TMSCN) (69.3 g, 0.7 mol) was added to a solution of 4-chloro-5-(chloromethyl)-2-(trifluoromethyl)pyridine (Int-13) (80 g, 0.348 mol) and Tetra-n-butylammoniumfluoride (129.5 g, 0.7 mol) in acetonitrile (1.5 L) slowly. Then the mixture was stirred at 20-30° C. for 2 hours. Thin layer chromatography (petroleum ether: EtOAc=3:1) showed all of starting material was consumed. The mixture was concentrated and the residue was purified by silica gel chromatography eluted with petroleum ether: EtOAc=20:1˜3:1 to yield [4-chloro-6-(trifluoromethyl)pyridin-3-yl]acetonitrile (Int-14) (50 g, 60% from NMR, 39% of yield) as yellow syrup.