![](/CAS/GIF/288399-90-6.gif)
6-FLUORO-4-METHYLCOUMARIN-3-CARBONITRIL& synthesis
- Product Name:6-FLUORO-4-METHYLCOUMARIN-3-CARBONITRIL&
- CAS Number:288399-90-6
- Molecular formula:C11H6FNO2
- Molecular Weight:203.17
![1-(5-Fluoro-2-hydroxyphenyl)-1-ethanone](/CAS/GIF/394-32-1.gif)
394-32-1
345 suppliers
$9.00/5g
![Cyanoacetic acid](/CAS/20180808/GIF/372-09-8.gif)
372-09-8
349 suppliers
$24.73/10gm:
![6-FLUORO-4-METHYLCOUMARIN-3-CARBONITRIL&](/CAS/GIF/288399-90-6.gif)
288399-90-6
19 suppliers
$75.00/500mg
Yield:288399-90-6 92%
Reaction Conditions:
with 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide;triethylamine in acetic acid butyl ester;ethyl acetate at 120;Perkin condensation;
Steps:
General procedure: T3P mediated synthesis of coumarins: To a mixture of 2-hydroxyaryl aldehyde/ketone (1, 0.01 mol) and appropriate acetic acid (2, 0.01 mol) in n-BuOAc (10 mL) was added T3P (0.02 mol, 50% soln in EtOAc) followed by triethylamine (0.02 mol). The resulting reaction mixture was stirred at 120 °C for 6-10 h under conventional heating. When the reaction was completed (monitored by TLC), the mixture was cooled and washed with saturated NaHCO3 solution (1 × 10 mL), water and brine. The organic phase was dried over anhydrous Na2SO4. The solvent was removed under reduced pressure and the crude product was passed through a small plug of silica to afford the coumarins (3) in good purity and yield.
References:
Augustine, John Kallikat;Bombrun, Agnes;Ramappa, Balakrishna;Boodappa, Chandrakantha [Tetrahedron Letters,2012,vol. 53,# 33,p. 4422 - 4425] Location in patent:experimental part
![1-(5-Fluoro-2-hydroxyphenyl)-1-ethanone](/CAS/GIF/394-32-1.gif)
394-32-1
345 suppliers
$9.00/5g
![Ethyl cyanoacetate](/CAS/GIF/105-56-6.gif)
105-56-6
431 suppliers
$10.00/5ml
![6-FLUORO-4-METHYLCOUMARIN-3-CARBONITRIL&](/CAS/GIF/288399-90-6.gif)
288399-90-6
19 suppliers
$75.00/500mg