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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72238생성일: 2026년 10월 24일

Diisopropylamine → 5-Formyl-3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/72238

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물1-PiperidinecarboxaldehydeHCID 17429—
반응물Ammonium ChlorideHCID 25517—
반응물Methyl 3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylateHCID 2805185—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물5-Formyl-3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl esterHCID 57618725—

반응 조건

온도0 °C

반응 단계

A 1.6M n-BuLi solution in hexane (12 mL) was added dropwise to a solution of diisopropylamine (2.9 mL) in THF (30 mL) at −78° C. The reaction mixture was stirred at 0° C. for 10 min and then cooled to −78° C., and a solution of 3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl ester (1.5 g) in THF (15 mL) was added. The reaction mixture was stirred at −78° C. for 30 min and then 1-formylpiperidine (4 g) was added, and the mixture was again stirred at this temperature for 1.5 h. Subsequently, saturated ammonium chloride solution was added and the reaction mixture was allowed to reach room temperature. The aqueous phase was extracted several times with ethyl acetate. The combined organic phases were dried over sodium sulfate and the solvent was removed in vacuo. The product with the molecular weight of 281.0 (C9H6F3NO4S) was obtained in this way; MS (ESI): 282 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828991B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-063af6f49cc04f6fbaaa08dfff6a4a13
출처 메모uspto-grants-2014_09