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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6972생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Potassium HydroxideHCID 14797—
반응물Methyl ThioglycolateHCID 16907—
반응물3-Methoxy-4,4,4-trifluoro-2-butenoic acid ethyl esterHCID 2758867—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물Methyl 3-hydroxy-5-(trifluoromethyl)thiophene-2-carboxylateHCID 275985591.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084170B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-3615251532314f45bc7131ceaf9195cd
출처 메모uspto-grants-2006_08