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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2245757Erstellt: 25. Oktober 2026

p-Chlorothiophenol → 6-(4-Chlorophenylsulfanyl)-hexa-2,4-dienoic acid methyl ester

https://huagongshe.com/reaction/2245757

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-ChlorothiophenolHCID 7815—
EduktTriethylamineHCID 8471—
Eduktt-Butylammonium IodideHCID 22344722—
EduktMethyl 6-bromohexa-2,4-dienoateHCID 54529347—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-(4-Chlorophenylsulfanyl)-hexa-2,4-dienoic acid methyl esterHCID 8597346463%

Reaktionsschritte

To a solution of 6-bromohexa-2,4-dienoic acid methyl ester (1.03 g, 5 mmol), triethylamine (1.4 mL, 10 mmol) and tert-butylammonium iodide (92 mg, 0.25 mmol) in freshly distilled THF (25 mL) was added 4-chlorothiophenol under an atmosphere of nitrogen. The mixture was stirred at reflux for 2 hours after which it was concentrated under reduced pressure. The oil was dissolved in, ethyl acetate (100 mL) and then washed successively with saturated aqueous sodium hydrogen carbonate (50 mL), distilled water (50 mL) and brine (50 mL). The organic layer was then dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to give an oil that was purified by flash chromatography (1:9 diethyl ether:40-60° C. petroleum ether). The resulting yellow solid was recrystallised from diethyl ether/40-60° C. petroleum ether to give the title compound (0.85 g, 63%) as a white solid, mp 75-77° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07683185B2
Quelldatensatzuspto-grants-2010_03
ORD IDord-d04c1471a40c46ab890045305b9cd2bf
Quellennotizuspto-grants-2010_03