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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6972Erstellt: 24. Oktober 2026

Sulfuric Acid → Methyl 3-hydroxy-5-(trifluoromethyl)thiophene-2-carboxylate

https://huagongshe.com/de/reaction/6972

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktPotassium HydroxideHCID 14797—
EduktMethyl ThioglycolateHCID 16907—
Edukt3-Methoxy-4,4,4-trifluoro-2-butenoic acid ethyl esterHCID 2758867—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
ProduktMethyl 3-hydroxy-5-(trifluoromethyl)thiophene-2-carboxylateHCID 275985591,2%

Reaktionsschritte

A solution of 4,4,4-trifluoro-3-methoxy-but-2-enoic acid ethyl ester (9.6 g, 48.5 mmol) and methyl thioglycolate (4.3 mL, 48.5 mmol) in MeOH (75 mL) is cooled to 5° C. A solution of KOH (3.3 g, 58.2 mmol) in MeOH (75 mL) is then added over 30 min. The reaction mixture is stirred overnight at room temperature. The reaction mixture is then poured over a stirred mixture of ice (75 g), H2O (75 mL) and concentrated H2SO4 (4.5 mL). The mixture is extracted with EtOAc (2×250 mL). The combined extracts are washed with saturated NaHCO3. The washings are back-extracted with EtOAc. The combined organic layers are washed with brine, then dried (Na2SO4), filtered and concentrated to afford the title compound (10 g, 91%) as a brown oil which is used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084170B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-3615251532314f45bc7131ceaf9195cd
Quellennotizuspto-grants-2006_08