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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127502Erstellt: 26. Oktober 2026

Trans-beta-dimethylamino-4-methyl-2-nitrostyrene → 1H-Indole, 6-methyl-

https://huagongshe.com/reaction/127502

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrans-beta-dimethylamino-4-methyl-2-nitrostyreneHCID 20550574—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelBenzeneHCID 241—
Produkt1H-Indole, 6-methyl-HCID 13792883%

Reaktionsschritte

A glass-lined rocking autoclave was charged with a solution of 300 g (1.45 moles) of trans-β-dimethylamino-4-methyl-2-nitrostyrene in 3 l of benzene and 15 g of 5% palladium on carbon. The autoclave was pressurized with 20 psi of hydrogen and rocked for 5 hours. The mixture was filtered through a bed of Celite, which was washed thoroughly with benzene. The filtrate was concentrated to half its volume and washed with 1 l of 0.25 N hydrochloric acid, 500 ml of saturated sodium bicarbonate and 500 ml of brine. The aqueous phases were backwashed with 500 ml of benzene and the combined organic phases were dried over sodium sulfate and concentrated. The residual dark brown oil was distilled at vacuo to afford 157.9 g (83%) of product as a light yellow oil, b.p. 80°-85°/0.05 mmHg, which solidified after seeding to a light yellow solid. m.p. 29°-30.5°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04256641
Quelldatensatzuspto-grants-1981_03
ORD IDord-7e4f4abd55a245a08e9d3bf59b6bbdea
Quellennotizuspto-grants-1981_03