Potassium Phosphate, Tribasic → HCID 86758107, compound
Reaction equation
FC(F)(F)S(O/[CH:7]=[CH:8]\[C:9]([O:11][CH2:12][CH3:13])=[O:10])(=O)=O.P([O-])([O-])([O-])=O.[K+].[K+].[K+].[C:24]([C:26]1[CH:27]=[C:28](B(O)O)[CH:29]=[CH:30][CH:31]=1)#[N:25]>O1CCOCC1>[C:24]([C:26]1[CH:31]=[C:30](/[CH:7]=[CH:8]\[C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH:29]=[CH:28][CH:27]=1)#[N:25]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of ethyl (Z)-3-{[(trifluoromethyl)sulfonyl]-oxy}-2-propenoate (330 mg, 1.25 mmol) in 5 ml anhydrous dioxane was added potassium phosphate (398 mg, 1.88 mmol), 3-cyanophenyl boronic acid (185 mg, 1.25 mmol), and tetrakis (triphenylphosphine)palladium(0) (36 mg, 0.031 mmol). Reaction mixture was heated to reflux and stirred overnight. Mixture was filtered through a pad of Celite, diluted with 50 ml ethyl acetate, washed with 2×50 ml water, 2×50 ml saturated brine solution, dried over magnesium sulfate, filtered and concentrated in vacuo. Residue was chromatographed on silica gel using 5% EtOAc in hexane as the eluent to give ethyl (Z) 3-(3-cyanophenyl)-2-propenoate (240 mg, 71%) as a clear oil after drying. ES-MS (M+H+): 216.05
Workup
- customReaction mixture
- temperaturewas heated
- temperatureto reflux
- filtrationMixture was filtered through a pad of Celite
- additiondiluted with 50 ml ethyl acetate
- washwashed with 2×50 ml water, 2×50 ml saturated brine solution
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customResidue was chromatographed on silica gel using 5% EtOAc in hexane as the eluent
Sources & evidence
- ORD record
- ord-0c7f3240a5974cbb83b625ea2f99ea2f
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06399627B1
Reaction notes
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