HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561916Erstellt: 26. Oktober 2026
Benzyl Bromide → 4-(Benzyloxy)-2-hydroxy-3-methylbenzaldehyde
https://huagongshe.com/reaction/561916
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Edukt | 2,4-Dihydroxy-3-methylbenzaldehyde | HCID 80395 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-(Benzyloxy)-2-hydroxy-3-methylbenzaldehyde | HCID 59761690 | — |
Reaktionsschritte
A mixture of 2,4-dihydroxy-3-methyl-benzaldehyde (3.31 g, 21.8 mmol), benzylbromide (4.09 g, 23.9 mmol), NaHCO3 (5.49 g, 65.4 mmol), 1,4-dioxane (30 mL) and water (12 mL) was stirred at 60° C. for overnight. Then the reaction mixture was cooled to RT, water (100 mL) was added, extracted with EtOAc (2×200 mL). The extract was dried over Na2SO4, evaporated. The residue was purified on SiO2 (25 g) column, hexane-EtOAc (0 to 5%). Yield 1.57 g (6.48 mmol, 29%) as off-white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08063225B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-4e2869e8413849ad91e67fd6dc8aed26 |
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| Quellennotiz | uspto-grants-2011_11 |
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