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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1452349Erstellt: 25. Oktober 2026

5-Benzyloxy-4-t-butyl-2-formylbenzofuran → 4-Tert-butyl-5-hydroxy-2-hydroxymethyl-2,3-dihydrobenzofuran

https://huagongshe.com/reaction/1452349

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Benzyloxy-4-t-butyl-2-formylbenzofuranHCID 23442879—
KatalysatorPalladiumHCID 23938—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Tert-butyl-5-hydroxy-2-hydroxymethyl-2,3-dihydrobenzofuranHCID 2291865787,2%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05606089
Quelldatensatzuspto-grants-1997_02
ORD IDord-3f44cac1eba74379bf4899f9af0b5788
Quellennotizuspto-grants-1997_02