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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785147Generated: October 30, 2026

Diisopropylamine → 5-Chloro-7-(4-methoxypent-1-yn-1-yl)-1,3-benzodioxol-4-amine

https://huagongshe.com/reaction/1785147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant5-Chloro-7-iodo-1,3-benzodioxol-4-amineHCID 17980527—
Reactant4-Methoxypent-1-yneHCID 86601564—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
Product5-Chloro-7-(4-methoxypent-1-yn-1-yl)-1,3-benzodioxol-4-amineHCID 6888121792%

Reaction Steps

5-chloro-7-iodo-1,3-benzodioxol-4-amine (600 mg, 2.02 mmol) and 4-methoxypent-1-yne (500 mg, 5.10 mmol) in ethyl acetate (8 ml) were cooled in ice-methanol, under an atmosphere of nitrogen, then treated with bis(triphenylphosphine)palladium(II) dichloride (141 mg, 10 mol %) followed by copper(I) iodide (38 mg, 10 mol %) and diisopropylamine (407 mg, 5.69 mmol). The reaction was allowed to warn to room temperature and stirred 90 min then filtered through Celite. The filtrate was purified by column chromatography on silica using a 1:1 mixture of methyl tert-butyl ether and iso-hexane as eluent to give 5-chloro-7-(4-methoxypent-1-yn-1-yl)-1,3-benzodioxol-4-amine (495 mg, 92%) as a dark brown oil;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504408B2
Source datasetuspto-grants-2009_03
ORD IDord-64136a8cd324442f9a988bcc15cbb60e
Source noteuspto-grants-2009_03