HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38718Erstellt: 23. Oktober 2026
Allyl bromide → 3-Chloro-4-(prop-2-en-1-yloxy)benzaldehyde
https://huagongshe.com/de/reaction/38718
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Allyl bromide | HCID 7841 | — |
| Edukt | 3-Chloro-4-hydroxybenzaldehyde | HCID 17022 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Produkt | 3-Chloro-4-(prop-2-en-1-yloxy)benzaldehyde | HCID 4770036 | 85,6% |
Reaktionsschritte
To a solution of 3-chloro-4-hydroxybenzaldehyde (5.0 g, 31.9 mmol) in DMF/THF 1:3 (120 mL) is added NaH (1.67 g of a 55% dispersion in mineral oil, 38.3 mmol) in four portions. The mixture is stirred at rt for 1 h before allylbromide (9.66 g, 79.8 mmol) is added. The reaction mixture is heated to 65° C. for 18 h, diluted with water (250 mL) and extracted with diethyl ether (3×250 mL). The organic extracts are washed with water (250 mL), combined and concentrated. The remaining oil is chromatographed on silic gel with heptane/EA 4:1 to afford 4-allyloxy-3-chlorobenzaldehyde (5.37 g) as an almost colourless oil. LC: tR=0.95 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524752B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-482bcd3dcc48433ea236a8b74dc6f9fd |
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| Quellennotiz | uspto-grants-2013_09 |
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