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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649Generated: October 25, 2026

N,N-Dimethylethylenediamine → N-(4-bromo-3-methoxyphenyl)-N',N'-dimethylethane-1,2-diamine

https://huagongshe.com/reaction/649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylethylenediamineHCID 66053—
Reactant1-Bromo-4-iodo-2-methoxybenzeneHCID 12187202—
ReagentSodium t-butoxideHCID 23676156—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductN-(4-bromo-3-methoxyphenyl)-N',N'-dimethylethane-1,2-diamineHCID 8286802045.64%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 1-bromo-4-iodo-2-methoxybenzene (0.63 g, 2.01 mmol) dissolved in toluene (15.73 ml) was treated with N1,N1-dimethylethane-1,2-diamine (0.177 g, 2.01 mmol), SODIUM TERT-BUTOXIDE (0.232 g, 2.42 mmol), XANTPHOS (0.116 g, 0.20 mmol) and TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.046 g, 0.05 mmol) under nitrogen. The resulting mixture was stirred at 80 °C in a sealed tube for 2 hours. The reaction mixture was diluted with water (200 mL), and extracted with ethyl acetate (200 mL). The organic was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution 0-10% methanol in dcm. Pure fractions were evaporated to dryness to afford N1-(4-bromo-3-methoxyphenyl)-N2,N2-dimethylethane-1,2-diamine (0.251 g, 45.6 %) as a brown oil.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-a7c71c7b356644fcbb6f6b90814539ca
Source note750 AstraZeneca ELN dataset