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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785090Generated: October 30, 2026

Diisopropylamine → 5-Chloro-7-(3-methoxyprop-1-ynyl)-1,3-benzodioxol-4-amine

https://huagongshe.com/reaction/1785090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant3-MethoxypropyneHCID 69393—
Reactant5-Chloro-7-iodo-1,3-benzodioxol-4-amineHCID 17980527—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
Product5-Chloro-7-(3-methoxyprop-1-ynyl)-1,3-benzodioxol-4-amineHCID 21082716—

Reaction Steps

Bis(Triphenyl-phosphine)palladium(II) chloride (472 mg), copper iodide (192 mg) and diisopropylamine (680 mg) were added to a stirred solution of 5-chloro-7-iodo-1,3-benzodioxol-4-amine (1000 mg) and methyl propargyl ether (471 mg) in ethyl acetate (10 mls) at −20° C. The reaction was allowed to warm to ambient temperature over 16 hours. The reaction mixture was partitioned between Ethyl acetate and saturated NaHCO3. The organics were washed with water and saturated brine and dried over magnesium sulfate. The product was purified by column chromatography on silica using a gradient of 80-100% Dichloromethane/isohexane as eluent. The 5-chloro-7-(3-methoxyprop-1-ynyl)-1,3-benzodioxol-4-amine product was thus obtained as a tan crystalline solid (200 mg); NMR Spectrum: (DMSOd6) 3.28 (s, 3H), 4.26 (s, 2H), 5.52 (s, 2H), 6.05 (s, 2H), 6.93 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504408B2
Source datasetuspto-grants-2009_03
ORD IDord-91b21b00d834420dbe555ee53af2550b
Source noteuspto-grants-2009_03