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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 527444Erstellt: 26. Oktober 2026

Water → methyl 2-(1-(4-chlorobenzoyl)-5-methoxy-1H-indol-3-yl)acetate

https://huagongshe.com/reaction/527444

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-Chlorobenzoyl chlorideHCID 8501—
EduktSodium hydrideHCID 24758—
Eduktmethyl 2-(5-methoxy-1H-indol-3-yl)acetateHCID 594955—
LösungsmittelDimethylformamideHCID 6228—
Produktmethyl 2-(1-(4-chlorobenzoyl)-5-methoxy-1H-indol-3-yl)acetateHCID 57563309—

Reaktionsschritte

Methyl 2-(5-methoxy-1H-indol-3-yl)acetate (60 mg, 0.27 mmol) and NaH (8 mg, 0.33 mmol) were stirred in anhydrous DMF (1 mL) at 0° C. under argon for 30 min, at which time 4-chlorobenzoyl chloride (57 mg, 0.33 mmol) was added. The reaction mixture was stirred overnight at room temperature and was then poured into cold water (2 mL). The organic compound was immediately extracted with dichloromethane (2×2 mL), dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified on silica (ethyl acetate/hexane gradient) and recrystallized from hexane. Yield: 18 mg (18%). C19H16ClNO4, Mr=357.79; 1H NMR (400 MHz, DMSO-d6) d: 3.61 (s, 3H), 3.78 (s, 2H), 3.81 (s, 3H), 7.00 (dd, J=2.4/9.0 Hz, 1H), 7.12 (d, J=2.4 Hz, 1H), 7.35 (s, 1H), 7.65-7.77 (m, 4H), 8.17 (d, J=8.8 Hz, 1H); LCMS (ESI) tR: 2.81 min (>99%, ELSD), m/z: 358.0 [M+1]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346803B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-64547cd1dbe042d9896b7a22cb3b889b
Quellennotizuspto-grants-2016_05