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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 587913Erstellt: 23. Oktober 2026

2-Bromopropane → 2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrile

https://huagongshe.com/de/reaction/587913

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromopropaneHCID 6358—
EduktAmmonium ChlorideHCID 25517—
Edukt3,4-DimethoxybenzeneacetonitrileHCID 66727—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrileHCID 89396—

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

To a solution of 9.99 g (56.4 mmol) of (3,4-Dimethoxyphenyl)acetonitrile in 141 mL of tetrahydrofuran (THF) at −30° C., was slowly added 56.4 mL (56.4 mmol) of sodium bis(trimethylsilyl)amide (NaHMDS, 1.0 M in THF). The mixture was stirred at −30° C. for 10 minutes and 10.6 mL (113.0 mmol) of 2-bromopropane was added. The mixture was heated to reflux for 2 hours (h) then left at 22° C. for about 16 h. A saturated aqueous solution of NH4Cl was 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 2-(3,4-dimethoxyphenyl)-3-methylbutanenitrile as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09227918B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-1de0264fd88043fa95c95fd18dd6fde3
Quellennotizuspto-grants-2016_01