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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238714생성일: 2026년 10월 26일

Hydrochloric Acid → 4-(3-Nitro-2-methoxy-phenyl)-thiophene-2-carboxylic acid

https://huagongshe.com/reaction/238714

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium CarbonateHCID 10340—
반응물4-Bromo-2-thiophenecarboxylic AcidHCID 610409—
반응물2-(2-Methoxy-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 57483800—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물4-(3-Nitro-2-methoxy-phenyl)-thiophene-2-carboxylic acidHCID 57483844133.4%

반응 단계

2-(2-Methoxy-3-nitro-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 4d (0.81 g, 2.9 mmol), 4-bromo-thiophene-2-carboxylic acid (0.3 g, 1.45 mmol), tetrakis (triphenylphosphine)palladium (80 mg, 0.073 mmol) and sodium carbonate (0.31 g, 2.9 mmol) were dissolved in a solvent mixture of 20 mL of 1,4-dioxane and 10 mL of water. The reaction was heated to reflux for 0.5 hours. The mixture was adjusted to pH 3 with 1 N hydrochloric acid and extracted with ethyl acetate (20 mL×3). The combined organic extracts were concentrated under reduced pressure and the residue was purified by silica gel column chromatography to obtain the title compound 4-(3-nitro-2-methoxy-phenyl)-thiophene-2-carboxylic acid 19a (0.54 g) as a brown oil, which was directly used in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642637B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-6b75d065aaba43979d898ef8c12a5b3e
출처 메모uspto-grants-2014_02