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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26478Erstellt: 24. Oktober 2026

Water → N-(3,3-dimethylallyl)-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline

https://huagongshe.com/de/reaction/26478

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukt2-Butene, 1-bromo-3-methyl-HCID 70092—
Edukt4a-(m-Methoxyphenyl)-1,3-diketo-trans-decahydroisoquinolineHCID 86736478—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-(3,3-dimethylallyl)-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinolineHCID 8673648094,4%

Reaktionsschritte

A solution of 4 g (14.7 mmoles) of 4a-(m-methoxyphenyl)-1,3-diketo-trans-decahydroisoquinoline in 50 ml of anhydrous dimethylformamide was added dropwise to 700 mg of a 55% suspension of sodium hydride in mineral oil in 50 ml of dimethylformamide at 70°. The reaction mixture was heated for 1 hour after the addition was complete and then cooled to 25°. 3,3-Dimethylallyl bromide (2.37 g, 15.8 mmoles) in 10 ml of dimethylformamide was added dropwise and the solution stirred overnight at 25°. After heating at 80° for 1 hour it was poured into water and extracted with ether to yield 4.74 g of N-(3,3-dimethylallyl)-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline (oil), which was evaporatively distilled, bp 225° (0.005 mm).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04150135
Quelldatensatzuspto-grants-1979_04
ORD IDord-c5f2f03608c945db9b80e903cc970a15
Quellennotizuspto-grants-1979_04