HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551973Generated: October 26, 2026
4-Iodoaniline → 4-(4-Butylphenylethynyl)phenylamine
https://huagongshe.com/reaction/551973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Iodoaniline | HCID 10893 | — |
| Reactant | 1-Butyl-4-ethynylbenzene | HCID 2775132 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(4-Butylphenylethynyl)phenylamine | HCID 57554509 | 48.5% |
Reaction Steps
To a stirred solution of 4-iodoaniline (20 g, 91 mmol, Aldrich) and 1-eth-1-ynyl-4-butylbenzene (16.7 g, 105 mmol, Aldrich) in dry acetonitrile (300 mL) under nitrogen was added CuI (0.83 g, 4.3 mmol), TEA (27.7 g, 273 mmol) followed by Pd(PPh3)2Cl2 (3 g, 4.3 mmol). The reaction mixture was stirred at 85° C. for 24 hours and the solvent was removed under reduced pressure. The residue was diluted with Et2O (200 mL) and washed with water, brine and dried (MgSO4). The solvent was removed under reduced pressure and the crude product was purified by chromatography (Pet Ether/EtOAc (4/1) to give 11 g (47%) of the title compound as a solid. TLC-Pet ether/EtOAc (4/1): Rf=0.35. HPLC purity >98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07947851B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-fe1046cc64df492b9b37fca70bdc3a8d |
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| Source note | uspto-grants-2011_05 |
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