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HRID 6972作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Potassium HydroxideHCID 14797—
反応物Methyl ThioglycolateHCID 16907—
反応物3-Methoxy-4,4,4-trifluoro-2-butenoic acid ethyl esterHCID 2758867—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物Methyl 3-hydroxy-5-(trifluoromethyl)thiophene-2-carboxylateHCID 275985591.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084170B2
出典データセットuspto-grants-2006_08
ORD IDord-3615251532314f45bc7131ceaf9195cd
出典メモuspto-grants-2006_08