Reaktionsgleichung
[I:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[CH:4][CH:3]=1.S(=O)(=O)(O)O.[CH3:19]O>>[I:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][CH2:10][C:11]([O:13][CH3:19])=[O:12])=[CH:6][CH:7]=1Komponenten
4
Versuchsvorschrift
To a solution of 4-(p-iodophenyl)-butyric acid (45.0 g, 0.155 mol) in methanol (1.3 L), was added sulfuric acid (concentrated, 8.4 mL) dropwise and it was stirred at room temperature under nitrogen for 3 hours. The reaction mixture was concentrated on a rota-vapor, the residue was then partitioned between ethyl acetate (700 mL) and saturated sodium bicarbonate aqueous solution (500 mL). The organic phase was separated, washed with brine (2×200 mL), then dried over Na2SO4 and filtered. Evaporation of solvent gave the titled compound as an oil that was used in step B without further purification.
Aufarbeitung
- concentrationThe reaction mixture was concentrated on a rota-vapor
- customthe residue was then partitioned between ethyl acetate (700 mL) and saturated sodium bicarbonate aqueous solution (500 mL)
- customThe organic phase was separated
- washwashed with brine (2×200 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- customEvaporation of solvent
Quellen und Nachweise
- ORD-Eintrag
- ord-ead1684ac2394d2d999f52d4ee7a9e11
- Quelldatensatz
- uspto-grants-2007_12
- Patentnummer
- US07304062B2
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