Triphenylphosphine → 3-Cyano-2-fluoropyridine
Reaction equation
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[F:20][C:21]1[N:29]=[CH:28][CH:27]=[CH:26][C:22]=1[C:23]([NH2:25])=O>ClC(Cl)C.C(Cl)(Cl)(Cl)Cl>[F:20][C:21]1[N:29]=[CH:28][CH:27]=[CH:26][C:22]=1[C:23]#[N:25]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Add resin bound triphenylphosphine (4.0 g, 12.0 mmol) to a solution of 2-fluoro-nicotinamide (0.6 g, 4.3 mmol) in dichloroethane (20.0 mL) and carbon tetrachloride (20.0 mL). Reflux for 18 hours, cool to RT, filter, and concentrate the filtrate under vacuum. Purify by flash column on silica gel eluting with 10-60% EtOAc in hexanes to give the title compound (0.34 g, 64%). MS (ES) 123.1 (M+1)+. 1H NMR (400 MHz, CHCl3) δ 8.46 (m, 1H), 8.09 (m, 1H), 7.37 (m, 1H).
Workup
- temperatureReflux for 18 hours
- filtrationfilter
- concentrationconcentrate the filtrate under vacuum
- customPurify by flash column on silica gel eluting with 10-60% EtOAc in hexanes
Sources & evidence
- ORD record
- ord-f785c08da873469b9a460065bb3c21ab
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07595339B2
Reaction notes
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