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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1362030Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1362030

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(o-Carboxyphenylthio)acetic acidHCID 8660—
EduktPhosphorus oxychlorideHCID 24813—
EduktChloro-N,N-dimethylformiminium chlorideHCID 77311—
LösungsmittelDimethylformamideHCID 6228—
ProduktChloro-N,N-dimethylformiminium chlorideHCID 77311—
Produkt3-Chloro-1-benzothiophene-2-carbaldehydeHCID 81812168%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07879872B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-c6ebb43eecd24317a3331641aa9a3d91
Quellennotizuspto-grants-2011_02