HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 356929Erstellt: 24. Oktober 2026
3-Chlorocyclopent-1-ene → 3-Cyclopent-2-enyloxy-4-methoxybenzaldehyde
https://huagongshe.com/de/reaction/356929
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Chlorocyclopent-1-ene | HCID 7297 | — |
| Edukt | Isovanillin | HCID 12127 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-Cyclopent-2-enyloxy-4-methoxybenzaldehyde | HCID 22145828 | — |
Reaktionsschritte
A solution of 3-hydroxy-4-methoxybenzaldehyde (14.20 g) in dry dimethylformamide (300 mL) is treated portionwise with sodium hydride (60% dispersion in oil; 3.70 g) at room temperature under nitrogen. 3-Chlorocyclo-pentene (9.6 mL) is added and the resulting mixture is stirred overnight. The solvent is then removed under reduced pressure and the residue is partitioned between water (500 mL) and dichloromethane (500 mL) and the aqueous layer is further extracted with dichloromethane (500 mL). The combined organic extracts are dried and evaporated under reduced pressure and the residue is subjected to flash chromatography on silica gel, eluting with a mixture of ethyl acetate and pentane (1:1 v/v), to give 3-cyclopent-2-enyloxy-4-methoxybenzaldehyde, in the form of a pale brown oil (11.2 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05840724 |
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| Quelldatensatz | uspto-grants-1998_11 |
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| ORD ID | ord-7f76afb33c724a78ab924db6c1a151ba |
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| Quellennotiz | uspto-grants-1998_11 |
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