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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41320Erstellt: 23. Oktober 2026

Benzaldehyde → 1,2-Diphenylethanol

https://huagongshe.com/de/reaction/41320

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktTetrahydrofuranHCID 8028—
EduktHCID 178419663HCID 178419663—
LösungsmittelSodium SulfateHCID 24436—
Produkt1,2-DiphenylethanolHCID 94178—

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

To 100 mL (0.10 mol) of 1.0 M BnMgBr in THF 9.50 g (90 mmol) of benzaldehyde (2) was added with vigorous stirring at −10° C. This mixture was slowly warmed to room temperature and then stirred for 2 hr at this temperature. The mixture was added to 300 mL of saturated aqueous Na2SO4. The organic layer was separated and washed with saturated aqueous NH4Cl. The aqueous layer was extracted with 2×100 mL of diethyl ether. The combined organic extracts were evaporated to dryness, and the residue was dissolved in 100 mL of dichloromethane. The obtained solution was dried over Na2SO4 and evaporated to dryness. This crude product was further used without an additional purification. Yield 12.0 g (67%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530593B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-a92efe51f65c46a4a278f1dc879cb1d8
Quellennotizuspto-grants-2013_09