Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347445Generated: October 30, 2026

Diisopropylamine → 4-(4-Methoxybut-1-yn-1-yl)-2,3-methylendioxyaniline

https://huagongshe.com/reaction/347445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant4-Methoxybut-1-yneHCID 542152—
Reactant7-Iodo-1,3-benzodioxol-4-amineHCID 22662750—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventEthyl AcetateHCID 8857—
Product4-(4-Methoxybut-1-yn-1-yl)-2,3-methylendioxyanilineHCID 2108270882%

Reaction Steps

A solution of 4-iodo-2,3-methylenedioxyaniline (1.32 g, 5.00 mmol) and 4-methoxybut-1-yne (0.84 g, 10.00 mmol) in ethyl acetate (25 ml) was cooled in ice-methanol, under an atmosphere of nitrogen, then treated with bis(triphenylphosphine) palladium(II) dichloride (350 mg, 10 mol %) followed by copper(I) iodide (95 mg, 10 mol %) and diisopropylamine (1.40 ml, 10.0 mmol). The reaction was stirred for 2 hours in the cooling bath and then allowed to warm to room temperature over 4 hours: The mixture was filtered through Celite and the filtrate was then purified by column chromatography on silica using a gradient of methanol in dichloromethane (0–2%) as eluent to give 4-(4-methoxybut-1-yn-1-yl)-2,3-methylendioxyaniline (524 mg, 82%) as a dark oil; LCMS: M+H+ 220 (82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173135B2
Source datasetuspto-grants-2007_02
ORD IDord-d9b71c28ada04a5b82e8ed3d6b9b6242
Source noteuspto-grants-2007_02