HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
5-Benzyloxy-4-t-butyl-2-formylbenzofuran → 4-Tert-butyl-5-hydroxy-2-hydroxymethyl-2,3-dihydrobenzofuran
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 5-Benzyloxy-4-t-butyl-2-formylbenzofuran | HCID 23442879 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4-Tert-butyl-5-hydroxy-2-hydroxymethyl-2,3-dihydrobenzofuran | HCID 22918657 | 87,2% |
Reaktionsschritte
5-Benzyloxy-4-tert-butyl-2-formylbenzofuran (5.0 g, 16 mmol) was dissolved in a 25:1 mixed solution (260 ml) of ethyl acetate and acetic acid. After adding 10% Pd on carbon (5.0 g), the solution was stirred under a hydrogen atmosphere for 48 h. After filtering off the Pd on carbon, the filtrate was washed with a saturated aqueous solution of sodium hydrogen carbonate, dried over anhydrous magnesium sulfate and concentrated. The concentrate was subjected to silica gel chromatography and eluted with a solvent system consisting of a 4:1 mixture of hexane and ethyl acetate to afford 4-tert-butyl-5-hydroxy-2-hydroxymethyl-2,3-dihydrobenzofuran [3.1 g (yield, 87%)] as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05606089 |
| Quelldatensatz | uspto-grants-1997_02 |
| ORD ID | ord-3f44cac1eba74379bf4899f9af0b5788 |
| Quellennotiz | uspto-grants-1997_02 |