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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 4-Methoxybut-1-yne | HCID 542152 | — |
| Reactant | 7-Iodo-1,3-benzodioxol-4-amine | HCID 22662750 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(4-Methoxybut-1-yn-1-yl)-2,3-methylendioxyaniline | HCID 21082708 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07173135B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-d9b71c28ada04a5b82e8ed3d6b9b6242 |
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| Source note | uspto-grants-2007_02 |
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