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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 587914Erstellt: 25. Oktober 2026

1,3-Dibromopropane → 5-Bromo-2-(3,4-dimethoxyphenyl)-2-isopropylpentanenitrile

https://huagongshe.com/reaction/587914

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-DibromopropaneHCID 8001—
EduktAmmonium ChlorideHCID 25517—
Edukt2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrileHCID 89396—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Bromo-2-(3,4-dimethoxyphenyl)-2-isopropylpentanenitrileHCID 13535571—

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

To a solution of 11.21 g (51.1 mmol) of 2-(3,4-dimethoxyphenyl)-3-methylbutanenitrile in 126 mL of tetrahydrofuran (THF) at −30° C., was slowly added 46.0 mL (46.0 mmol) of sodium bis(trimethylsilyl)amide (NaHMDS, 1.0 M in THF). The mixture was stirred at −30° C. for 10 minutes and 9.40 mL (256 mmol) of 1,3-dibromopropane was added dropwise. The mixture was warmed to 22° C. and stirred for about 16 h. A saturated aqueous solution of NH4Cl was then added and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried (Na2SO4), filtered and evaporated. The residue was purified by flash chromatography on silica gel eluting first with hexane and then gradually increasing to 15% ethyl acetate/hexane to give 5-bromo-2-(3,4-dimethoxyphenyl)-2-isopropylpentanenitrile as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09227918B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-10e46017d7674332baeb174f1751786b
Quellennotizuspto-grants-2016_01