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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1739786Erstellt: 25. Oktober 2026

Hexane → Ammonium Hydroxide

https://huagongshe.com/reaction/1739786

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
Edukt(+/-)-trans-1,2,3,4,4a,5,6,7,8,8a-Decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinoneHCID 10517409—
EduktButyllithiumHCID 178418339—
KatalysatorBenzyltriphenylphosphonium chlorideHCID 70671—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktAmmonium HydroxideHCID 14923—
Produkt(+/-)-trans-6-Benzylidene-1,2,3,4,4a,5,6,7,8,8a-decahydro-2-ethyl-4a-(3-methoxyphenyl)isoquinolineHCID 86754628—

Reaktionsschritte

9.9 ml (13.9 mmol) of a 1.4 M solution of n-butyllithium in hexane were added dropwise, under a nitrogen atmosphere and at room temperature, to a suspension of 5.4 g (13.9 mmol) of benzyltriphenylphosphonium chloride in 30 ml of dry THF. The reaction mixture was stirred for 1 h, then a solution of 1 g (3.5 mmol) of (±)-trans-1,2,3,4,4a,5,6,7,8,8a-decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinone in 10 ml of dry THF was added. The reaction mixture was refluxed 4 h, then cooled and poured onto water and the aqueous phase was extracted with AcOEt. The organic phase was dried over Na2SO4 and the solvent removed in vacuo. The crude reaction mixture was purified by flash chromatography, eluting with a mixture CH2Cl2 /MeOH/conc. NH4OH 90:7:0.7 respectively, yielding 0.94 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05968949
Quelldatensatzuspto-grants-1999_10
ORD IDord-8873cc4ed8fb4a249b44cb7f47806857
Quellennotizuspto-grants-1999_10