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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1362030생성일: 2026년 10월 25일

(o-Carboxyphenylthio)acetic acid → 3-Chloro-1-benzothiophene-2-carbaldehyde

https://huagongshe.com/reaction/1362030

반응식

참여 물질

역할이름HCID투입량
반응물(o-Carboxyphenylthio)acetic acidHCID 8660—
반응물Phosphorus oxychlorideHCID 24813—
반응물Chloro-N,N-dimethylformiminium chlorideHCID 77311—
용매DimethylformamideHCID 6228—
생성물Chloro-N,N-dimethylformiminium chlorideHCID 77311—
생성물3-Chloro-1-benzothiophene-2-carbaldehydeHCID 81812168%

반응 단계

Vilsmeier reagent was prepared via the dropwise addition of POCl3 (7.9 mL, 84 mmol) into ice-cold DMF (14 mL). A solution of 2-carboxymethylsulfanyl-benzoic acid (3.0 g, 14 mmol) in DMF (15 mL) was added dropwise to the Vilsmeier reagent. The resulting mixture was warmed to room temperature and then heated to 80° C. for 3.5 h. The reaction mixture was cooled to ambient temperature. Crushed ice was added until a bright yellow precipitate appeared. The solid was isolated by filtration. Purification by flash column chromatography (silica gel, hexanes/ethyl acetate 3:2) gave the title compound (1.87 g, 68%) as a yellow powder: 1H NMR (300 MHz, CDCl3) δ 10.36 (s, 1H), 8.03 (m, 1H), 7.86 (m, 1H), 7.59-7.53 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879872B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-c6ebb43eecd24317a3331641aa9a3d91
출처 메모uspto-grants-2011_02