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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587914Generated: October 25, 2026

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

https://huagongshe.com/reaction/587914

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrileHCID 89396—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-2-(3,4-dimethoxyphenyl)-2-isopropylpentanenitrileHCID 13535571—

Reaction Conditions

Temperature-30 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227918B2
Source datasetuspto-grants-2016_01
ORD IDord-10e46017d7674332baeb174f1751786b
Source noteuspto-grants-2016_01