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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22407Erstellt: 23. Oktober 2026

Potassium Hydroxide → 1-Amino-3-benzoylpyrrole

https://huagongshe.com/de/reaction/22407

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukthydroxylamine-O-sulfonic acidHCID 76284—
Edukt3-BenzoylpyrroleHCID 2773234—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Amino-3-benzoylpyrroleHCID 19973156—

Reaktionsschritte

To a solution of 3-benzoylpyrrole (4.92 g) in 50 ml of dry dimethylformamide was added milled potassium hydroxide (8.06 g). Hydroxylamine-O-sulfonic acid (4.23 g) was added to the suspension in 4 portions over a period of 1 hour with stirring at room temperature. After the addition was completed the reaction mixture was stirred for 30 minutes at room temperature, and subsequently diluted with 50 ml of water and extracted with DCM. The combined organic layers were washed with water, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by flash column chromatography (silica gel, DCM/ethyl acetate, 5:1), affording starting material (1.44 g) and the desired product as the second fraction. Recrystallization from ethyl ether/hexane gave the product as crystals (1.80 g), which was combined with material obtained from a 36.9 mmol scale reaction and recrystallized from DCM/hexane affording 3.20 g of crystals, m.p. 82°-83° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05428053
Quelldatensatzuspto-grants-1995_06
ORD IDord-10b426337f1a4e8d857367c3d6f38ad1
Quellennotizuspto-grants-1995_06