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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3572Erstellt: 24. Oktober 2026

Thionyl Chloride → 3-methoxy-4-nitro-benzoyl Chloride

https://huagongshe.com/de/reaction/3572

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThionyl ChlorideHCID 24386—
Edukt3-Methoxy-4-nitrobenzoic acidHCID 78764—
Produkt3-methoxy-4-nitro-benzoyl ChlorideHCID 1112765552,1%

Reaktionsschritte

A mixture of 5.0 g of 3-methoxy-4-nitrobenzoic acid and 5.0 g of thionyl chloride is heated under argon for 1 hour. The volatiles are removed in vacuo to give 2.85 g of a 3-methoxy-4-nitrobenzoyl chloride as a residue which is dissolved in 50 ml of methylene chloride. To the preceding solution is added with stirring 1.75 g of N,N-diisopropylethylamine followed by 1.84 g of 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine. The reaction mixture is stirred under argon for 18 hours and diluted with saturated sodium bicarbonate. The organic layer is dried with Na2 SO4 and passed through a short pad of hydrous magnesium silicate. While boiling, hexane is added to the filtrate to give, upon cooling, 3.39 g of the desired product as a solid, m.p. 191°-192° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05733905
Quelldatensatzuspto-grants-1998_03
ORD IDord-08380087dc6b4d579315e4dd8ce88d84
Quellennotizuspto-grants-1998_03