HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1670Erstellt: 23. Oktober 2026
Benzyl Bromide → Methyl 4-(benzyloxy)-2-hydroxybenzoate
https://huagongshe.com/de/reaction/1670
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Methyl 2,4-Dihydroxybenzoate | HCID 16523 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | Methyl 4-(benzyloxy)-2-hydroxybenzoate | HCID 225489 | — |
Reaktionsschritte
To a stirred, 0° C. solution of methyl 2,4-dihydroxybenzoate (50 g, 300 mmol) in acetone (1000 mL) was added K2CO3 (150 g, 1000 mmol) and benzyl bromide (330 mmol, 39 mL). The solution was allowed to warm to ambient temperature over 48 h. The reaction solution was filtered through celite and the acetone solution stripped down under reduced pressure. The crude oil was dissolved in EtOAc (1000 mL) and washed with water (250 mL), and saturated aqueous NaHCO3 (500 mL). The EtOAc layer was dried (MgSO4), filtered, and the EtOAc was removed under reduced pressure. The crude product was purified by pressurized silica gel column chromatography using 5:1 hexanes:EtOAc. Evaporation of the hexanes:EtOAc mixture gave the desired methyl 4-benzyloxy-2-hydroxybenzoate as a white powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05726172 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-b4fd402e735143d2ba1df2c8a9a0fe8f |
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| Quellennotiz | uspto-grants-1998_03 |
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