HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 594266Erstellt: 27. Oktober 2026
4-Hydroxybenzaldehyde → 4-(2-Fluoroethoxy)benzaldehyde
https://huagongshe.com/reaction/594266
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Ethane, 1-fluoro-2-iodo- | HCID 69804 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(2-Fluoroethoxy)benzaldehyde | HCID 15058649 | — |
Reaktionsschritte
A mixture of commercially available 4-hydroxybenzaldehyde (2.000 g; 16.40 mmol), 1-fluoro-2-iodoethane (2.849 g; 16.40 mmol), and K2CO3 (4.527 g; 32.80 mmol) in anh. DMF (30 ml) was heated to 70° C., under nitrogen, for 2.5 h. After cooling to rt, the reaction mixture was filtered over a pad of celite. Et2O was added and the organic layer was washed with water, dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure affording 4-(2-fluoroethoxy)benzaldehyde as a yellow oil. LC-MS (conditions A): tR=0.58 min.; no ionisation.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09242970B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-9eea868a239d40a6befda0c06afd9d43 |
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| Quellennotiz | uspto-grants-2016_01 |
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