HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1351657Erstellt: 26. Oktober 2026
3-Iodobenzaldehyde → 3-[(4-Bromophenyl)sulfonyl]benzaldehyde
https://huagongshe.com/reaction/1351657
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3-Iodobenzaldehyde | HCID 252610 | — |
| Edukt | Sodium 4-bromobenzene-1-sulfinate | HCID 23670685 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 3-[(4-Bromophenyl)sulfonyl]benzaldehyde | HCID 21099484 | 35,8% |
Reaktionsschritte
3-Iodobenzaldehyde (1.0 g, 4.3 mmol), copper(I) iodide (2.45 g, 12.9 mmol) and sodium 4-bromophenylsulfinate (1.55 g, 5.59 mmol) were combined in dimethylsulfoxide (8.6 mL) and heated to 110° C. for 4 hours. The cooled reaction mixture was diluted with ethyl acetate and filtered through Hyflo®. The filtrate was washed with water (×2) and brine and dried over MgSO4. The solvent was removed in vacuo and the residue purified by flash column chromatography on silica, eluting with 25% ethyl acetate/isohexane, to give 3-[(4-bromophenyl)sulfonyl]benzaldehyde (0.5 g, 35%). δH (400 MHz, d6 DMSO): 10.09 (1H, s), 8.47–8.44 (1H, m), 8.29–8.25 (1H, m), 8.21 (1H, d, J=7.6 Hz), 7.96–7.94 (2H, m), 7.88–7.84 (3H, m).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07217740B2 |
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| Quelldatensatz | uspto-grants-2007_05 |
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| ORD ID | ord-38ca2c63ebc34dd4ad58df02e7fe49f2 |
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| Quellennotiz | uspto-grants-2007_05 |
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