HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 496179Erstellt: 26. Oktober 2026
Dimethyl Sulfoxide → 3-Fluorobenzene-1,2-dicarbaldehyde
https://huagongshe.com/reaction/496179
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | 2,5-Difluorobenzaldehyde | HCID 137663 | — |
| Edukt | Dilithium Sulfide | HCID 10290727 | — |
| Produkt | 3-Fluorobenzene-1,2-dicarbaldehyde | HCID 22325230 | 59% |
Reaktionsschritte
To a stirred solution of 17.5 g (123 mmol) of 2,5-difluorobenzaldehyde (Aldrich) in 615 mL of DMSO at ambient temperature was added 6.2 g (135 mmol) of lithium sulfide (Aldrich). The dark red solution was stirred at 75 C for 1.5 hours, or until the starting material was completely consumed, and then 34 g (135 mmol) of dibutyl mesylate aldehyde was added at about 50 C. The reaction mixture was stirred at 75 C for three hours or until the reaction was completed. The cooled solution was poured into water and extracted with ethyl acetate. The combined extracts were washed with water several times, dried (MgSO4) and concentrated in vacuo. Silica gel chromatographic purification of the crude product gave 23.6 g (59%) of fluorobenzene dialdehyde as a yellow oil: 1H NMR (CDCl3) d 0.87 (t, J=7.05 Hz, 6H), 1.0-1.4 (m, 8H), 1.5-1.78 (m, 4H), 3.09 (s, 2H), 7.2-7.35 (m, 1H), 7.5-7.6 (m, 2H), 9.43 (s, 1H) 10.50 (d, J=2.62 Hz, 1H)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06943189B2 |
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| Quelldatensatz | uspto-grants-2005_09 |
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| ORD ID | ord-19c0894312d14027be594246d09d1d8d |
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| Quellennotiz | uspto-grants-2005_09 |
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