Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1109666Erstellt: 25. Oktober 2026

1,2-Epoxybutane → 3-Phenyl-2(S)-phthalimidopropan-1-al

https://huagongshe.com/reaction/1109666

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-EpoxybutaneHCID 7834—
EduktSodium PyrosulfiteHCID 656671—
Edukt3-phenyl-2(S)-phthalimidopropionyl chlorideHCID 10567197—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt3-Phenyl-2(S)-phthalimidopropan-1-alHCID 1106580170%

Reaktionsschritte

1 mol of 1,2-butylene oxide and 23.5 g of Pd/C (5% Pd) were added to a solution of 0.5 mol of 3-phenyl-2(S)-phthalimidopropionyl chloride in 1200 ml of toluene. The suspension was hydrogenated at room temperature and atmospheric pressure while stirring vigorously for 17 hours, whereby 11.3 l of hydrogen were taken up. Thereafter, the suspension was filtered over a filter aid and the residue was washed with toluene. The filtrate and washings were combined and treated while stirring with a solution of 0.5 mol of sodium pyrosulphite in 1 l of water. After stirring at room temperature for 4.5 hours the phases were separated. The aqueous phase was washed with 500 ml of toluene. The toluene phases were washed with 350 ml of water. The combined aqueous phases were treated with 1400 ml of toluene and 420 ml of 3N sulphuric acid and stirred at 60° for 6 hours. Thereafter, the phases were separated and the aqueous phase was extracted with 500 ml of toluene. The toluene phases were washed with water, combined, dried over MgSO4 and evaporated. There were obtained 97.8 g (70%) of (S)-α-benzyl-1,3-dioxo-2-isoindolineacetaldehyde as a white solid, melting point 115°-117°, [α]D20 -200° (1% in ethyl acetate).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05321166
Quelldatensatzuspto-grants-1994_06
ORD IDord-6f2ab25ca6a94323992c7ceca80a89bb
Quellennotizuspto-grants-1994_06