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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981557Generated: November 3, 2026

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

https://huagongshe.com/reaction/1981557

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantSodium HydroxideHCID 14798—
Reactant3,4-DimethoxybenzeneacetonitrileHCID 66727—
CatalystBenzyl triethylammonium chlorideHCID 66133—
Product2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrileHCID 8939657.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

27.83 g of 50% NaOH solution, 5.84 g (145.95 mmol) of NaOH pellets and veratryl cyanide (8.9 g, 50.24 mmol) were placed in a 100 ml round-bottom flask. 2.05 g (9.02 mmol) of TEBAC was added and the mixture was stirred until homogenous while heating to 50° C. with a heating mantle. Isopropyl bromide (5.5 ml, 58.58 mmol) was added dropwise over 0.5 h at 50° C.±5° to the above mixture which was stirred at 50° C.±5° for 24 hours. The reactin mixture was partitioned between water and toluene and transferred to a separatory funnel. The aqueous layer was drawn off and extracted with ether. The toluene and ether fractions were combined and washed twice with water and dried over Na2SO4. The mixture was filtered and solvent removed by rotary evaporation. The combined fractions, following evaporation and recrystallization from 70 percent methanol/water yielded 6.32 g of the title compound (57% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04593042
Source datasetuspto-grants-1986_06
ORD IDord-90f2a251eeb5431f9e3327dce5c3f8eb
Source noteuspto-grants-1986_06