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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587913Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantAmmonium ChlorideHCID 25517—
Reactant3,4-DimethoxybenzeneacetonitrileHCID 66727—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
SolventTetrahydrofuranHCID 8028—
Product2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrileHCID 89396—

Reaction Conditions

Temperature-30 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227918B2
Source datasetuspto-grants-2016_01
ORD IDord-1de0264fd88043fa95c95fd18dd6fde3
Source noteuspto-grants-2016_01