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HRID 22399Erstellt: 23. Oktober 2026

Tin tetrachloride → 2-[(3-Methyl-2-thienyl)carbonyl-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H)dion

https://huagongshe.com/de/reaction/22399

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTin tetrachlorideHCID 24287—
EduktOxalyl chlorideHCID 65578—
Edukt3-Methyl-2-thenoic acidHCID 90269—
Edukt2-(1H-Pyrrol-1-yl)isoindoline-1,3-dioneHCID 853719—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-[(3-Methyl-2-thienyl)carbonyl-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H)dionHCID 1997316025,2%

Reaktionsschritte

To a stirred solution consisting of 3-methyl-2-thiophenecarboxylic acid (21.0 g) in dry DCM (1.5 l) was added oxalyl chloride (21.0 ml) at room temperature under nitrogen. After stirring for 1 hour at room temperature, the reaction mixture was cooled to -10° C. and tin (IV) chloride (17.3 ml) was added. The resulting solution was stirred for 10 minutes (-10° C.) at which time 2-(1H-pyrrol-1-yl)-1H-isoindole-1,3(2H)dione (31.3 g) was added in three portions. After stirring for 1 hour in the cooling bath, the reaction mixture was poured into cold water and the layers separated. The organic phase was washed twice with 5% HCl (aq.) and dried (MgSO4). Filtration and concentration gave the crude product. Purification via preparative HPLC (silica gel, DCM) afforded 12.5 g of the product as a solid, m.p. 221°-223° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05428053
Quelldatensatzuspto-grants-1995_06
ORD IDord-2cae46611d054557b1f2884d62f68941
Quellennotizuspto-grants-1995_06