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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1836712Erstellt: 25. Oktober 2026

Acetic Anhydride → HCID 11725738, Verbindung

https://huagongshe.com/reaction/1836712

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt1-(Phenylsulfonyl)-1H-indole-2-carbaldehydeHCID 2776223—
EduktHCID 178461836HCID 178461836—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 11725738HCID 11725738—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 2.9 g (10 mmol) of 1-benzenesulfonyl-1H-indole-2-carbaldehyde (synthesized analogous to M. G. Saulnier, G. W. Gordon, J. Org. Chem.; 47; 5; 1982, 757-761) in 10 ml of tetrahydrofuran was added 6.5 ml of vinylmagnesium chloride 1.7 M solution in THF at −20° C. within 1 h. The temperature increased to 0° C. within 30 min and kept at this temperature for 20 min. To the suspension 1.3 ml acetic anhydride (14 mmol was added at 0° C. within 15 min. The cooling bath was removed and after stirring for 1 h at 20° C. 10 ml water was added at 10-15° C. The mixture was stirred for an additional 1 h at 20° C. The phases were separated, and the aqueous phase was extracted with 20 ml of ethyl acetate. The combined organic phases were washed with 20 ml of brine, dried on sodium sulfate and rotary evaporated (35° C., 12 mbar). The crude material was purified by liquid chromatography (eluent isohexane/ethyl acetate 9:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06777559B2
Quelldatensatzuspto-grants-2004_08
ORD IDord-77fda8706381400ea6a76bee3cd4533e
Quellennotizuspto-grants-2004_08