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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1877215생성일: 2026년 10월 26일

Hydrochloric Acid → 2,5-Dimethylthiophene-3-carbaldehyde

https://huagongshe.com/reaction/1877215

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2,5-Dimethylthiophene-3-carboxylic acidHCID 819559—
촉매HCID 178418406HCID 178418406—
용매TetrahydrofuranHCID 8028—
생성물2,5-Dimethylthiophene-3-carbaldehydeHCID 276275968.1%

반응 단계

To a solution (20 mL) of 2,5-dimethylthiophene-3-carboxylic acid (920 mg) in tetrahydrofuran was added 1.0M borane-tetrahydrofuran complex in tetrahydrofuran solution (7.07 mL) at 0° C., and the mixture was stirred at room temperature overnight. 1.0M Borane-tetrahydrofuran complex in tetrahydrofuran solution (14.1 mL) was added, and the mixture was further stirred at room temperature for 3 hr. 1N Hydrochloric acid was added to quench the reaction, tetrahydrofuran was evaporated using evaporator, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by NH-silica gel column chromatography (ethyl acetate:hexane=2:3, volume ratio) to give a yellow oil. To a solution of the obtained oil in tetrahydrofuran (10 mL) was added activated manganese dioxide (3.32 g), and the mixture was stirred at room temperature overnight. Manganese dioxide was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (562 mg, 68%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309580B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-d45f36f8c436453abfba0f6207353c3b
출처 메모uspto-grants-2012_11