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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 260588Erstellt: 25. Oktober 2026

2,3-Dihydroxybutanedioic Acid → 4-Formylbenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether

https://huagongshe.com/reaction/260588

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-Dihydroxybutanedioic AcidHCID 875—
EduktSodium SulfateHCID 24436—
Edukt4-Cyanobenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl etherHCID 14850577—
EduktDiisobutylaluminumhydrideHCID 21225700—
LösungsmittelDiethyl EtherHCID 3283—
Produkt4-Formylbenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl etherHCID 14850579—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

15.5 ml (19.7 mmol) of diisobutylaluminum hydride solution (20% in hexane) were added dropwise under nitrogen to a solution of 3 g (9.4 mmol) of 4-cyanobenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl ether in 40 ml of dry ether at 25° C. The mixture was stirred at 25° C. for 40 min and then 250 ml of saturated tartaric acid solution were added dropwise. Subsequently, a little sodium sulfate solution was added, and the phases were separated. The aqueous phase was extracted with ether, and the organic extract was washed with saturated tartaric acid solution and water, dried over Na2SO4 and concentrated. Recrystallization from methanol resulted in 1.4 g of the title compound of melting point 102°-104° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05527945
Quelldatensatzuspto-grants-1996_06
ORD IDord-9b1e58a9d890461b98713f01079a85cd
Quellennotizuspto-grants-1996_06