HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409362Generated: October 28, 2026
1-Bromo-2-chloro-4-iodobenzene → 2-(4-Bromo-3-chlorophenyl)thiophene
https://huagongshe.com/reaction/409362
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-2-chloro-4-iodobenzene | HCID 2756886 | — |
| Reactant | 2-(Tri-n-butylstannyl)thiophene | HCID 2779373 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(4-Bromo-3-chlorophenyl)thiophene | HCID 57994054 | — |
Reaction Steps
To a mixture of 1-bromo-2-chloro-4-iodobenzene (2.0 g, 6.30 mmol) in dioxane 30 mL, 2-tributylstannyl thiophene (2.352 g, 6.30 mmol), and 5% equivalent of Pd(PPh3)4 (0.364 g, 0.3155 mmol) is refluxed under nitrogen for 5 h. After cooling and evaporation of the solvent, the residue is dissolved in EtOAc 50 mL. 10% KF 30 mL is added and the solution is stirred at r.t. for 30 min. The resultant precipitate is removed by filtration. The solution is washed with water 20 mL×3, and dried with Na2SO4 and concentrated. The pure product (1.2 g, 4.39 mmol, white solid) is obtained by column chromatography using EtOAc/Hexane, 1-3% ration solvent system. 1H-NMR (CDCl3/300 MHz): 7.74 (d, J=2.1 Hz, 1H), 7.65 (d, J=7.2 Hz, 1H), 7.37 (m, 3H), 7.14 (m, 1H). MS (ES−, m/z): 529.2 (M+−Br, 20.0).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759384B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-01825ac4a1b8463888a3bdc7b1eec4e0 |
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| Source note | uspto-grants-2014_06 |
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