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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 496161Erstellt: 23. Oktober 2026

Ethylacrolein → 2-((2-Benzoylphenylthio)methyl)butyraldehyde

https://huagongshe.com/de/reaction/496161

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylacroleinHCID 70203—
Edukt2-MercaptobenzophenoneHCID 3499713—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-((2-Benzoylphenylthio)methyl)butyraldehydeHCID 2232522364%

Reaktionsschritte

To an ice bath cooled solution of 9.76 g (0.116 mole) of 2-ethylacrolein in 40 mL of dry THF was added 24.6 g (0.116 mole) of 2-mercaptobenzophenone in 40 mL of THF followed by 13 g (0.128 mole) of triethylanine. The reaction mixture was stirred at room temperature for 3 days, diluted with ether, and was washed successively with dilute HCl, brine, and 1 M potassium carbonate. The ether layer was dried over MgSO4 and concentrated in vacuo. The residue was purified by HPLC (10% EtOAc-hexane) to give 22 g (64%) of 11 in the second fraction. An attempt to further purifiy this material by kugelronr distillation at 0.5 torr (160-190° C.) gave a fraction (12.2 g) which contained starting material indicating a reversed reaction during distillation. This material was dissolved in ether (100 mL) and was washed with 50 mL of 1 M potassium carbonate three times to give 6.0 g of a syrup which was purified by HPLC (10% EtOAc-hexane) to give 5.6 g of pure 11.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06943189B2
Quelldatensatzuspto-grants-2005_09
ORD IDord-82ef325b99484b92b22692152b474b38
Quellennotizuspto-grants-2005_09