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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1112015Erstellt: 26. Oktober 2026

2-(Cyclohexylthio)-1H-isoindole-1,3(2H)-dione → Phthalimide

https://huagongshe.com/reaction/1112015

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Cyclohexylthio)-1H-isoindole-1,3(2H)-dioneHCID 28777—
LösungsmittelHeptaneHCID 8900—
ProduktPhthalimideHCID 6809—

Reaktionsschritte

13.1 Grams (0.05 mole) of N-(cyclohexylthio)phthalimide and 6.9 grams (0.05 mole) of benzoyl thiol(thiobenzoic acid) in 150 ml of heptane are stirred overnight at room temperature. The precipitate is recovered by filtration, washed with carbon tetrachloride and dried. 7.3 Grams of phthalimide (m.p. 234° C.) are obtained. The solvent is removed from the filtrate by evaporation under reduced pressure. 12 Grams (95% yield) of product, a light brown liquid, are obtained. The identity of the benzoylcyclohexyl disulfide is confirmed by GLC and NMR analyses. Analysis gives 25.51% sulfur compared to 25.45% sulfur calculated for C13H16OS2. Similarly, except N-(2-benzothiazolylthio)phthalimide is one reactant, there is obtained benzoyl-2-benzothiazolyl disulfide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04119780
Quelldatensatzuspto-grants-1978_10
ORD IDord-a5361563754f43c99387715370b7a68e
Quellennotizuspto-grants-1978_10