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1-[4-(METHYLSULFANYL)PHENYL]-1,4-PENTANEDIONE synthesis

3synthesis methods
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Yield:189501-33-5 80%

Reaction Conditions:

with 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide;triethylamine at 70; under 7757.43 Torr; for 0.25 h;Microwave irradiation;Stetter 1,4-Dicarbonyl Synthesis;

Steps:

Synthesis of 1-[4-(methylthio)phenyl]pentane-1,4-dione (5).
A solution of 4-methylthiobenzaldehyde 4 (11.97 mL, 0.09 mol), triethylamine (19.5 mL, 0.14 mol), methyl vinyl ketone (5.8 mL, 0.09 mol), and 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide (3.53 g, 0.014 mol), in a 20 mL vial, was microwave irradiated using a CEM apparatus for 15 min at 70 °C (150 W, internal pressure of 150 psi). The reaction mixture was treated with 2 N HCl (10 mL) and extracted with ethyl acetate; the organic layer was washed with aqueous sodium bicarbonate and brine. The organic fractions were dried over sodium sulfate, filtered, and concentrated to give an orange liquid which was crystallized from cyclohexane to give intermediate 5 as white needles (80% yield). ESI-mass: m/z 245.063 [M+Na]+, mp, and 1H NMR spectrum were consistent with those reported in the literature. 16 and 23

References:

Battilocchio, Claudio;Poce, Giovanna;Alfonso, Salvatore;Porretta, Giulio Cesare;Consalvi, Sara;Sautebin, Lidia;Pace, Simona;Rossi, Antonietta;Ghelardini, Carla;Di Cesare Mannelli, Lorenzo;Schenone, Silvia;Giordani, Antonio;Di Francesco, Luigia;Patrignani, Paola;Biava, Mariangela [Bioorganic and Medicinal Chemistry,2013,vol. 21,# 13,p. 3695 - 3701]

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