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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1284607Erstellt: 25. Oktober 2026

Sulfuryl chloride → 1H-Isoindole-1,3(2H)-dione, 2-(4-chloro-2-fluoro-5-(1-methylethoxy)phenyl)-4,5,6,7-tetrahydro-

https://huagongshe.com/reaction/1284607

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuryl chlorideHCID 24648—
EduktN-(2-Fluoro-5-isopropoxyphenyl)-3,4,5,6-tetrahydrophthalimideHCID 13556385—
KatalysatorDicyclohexylamineHCID 7582—
LösungsmittelTetrachloroethyleneHCID 31373—
Produkt1H-Isoindole-1,3(2H)-dione, 2-(4-chloro-2-fluoro-5-(1-methylethoxy)phenyl)-4,5,6,7-tetrahydro-HCID 15865083,1%

Reaktionsschritte

N-(2-Fluoro-5-isopropoxyphenyl)-3,4,5,6-tetrahydrophthalimide (II: R=isopropyl) (2 g) and dicyclohexylamine (0.01 g) were dissolved in tetrachloroethylene (20 ml), and a solution of sulfuryl chloride (1 g) in tetrachloroethylene (5 ml) was added dropwise thereto at 80° C. in 2 hours. After completion of the addition, the resultant mixture was stirred at the same temperature as above for 2 hours, followed by extraction with ethyl acetate. The extract was concentrated, and the precipitated crystals were collected by filtration to give 1.85 g of N-(4-chloro-2-fluoro-5-isopropoxyphenyl)-3,4,5,6-tetrahydrophthalimide (I: R=isopropyl). M.P., 81°-82° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04563535
Quelldatensatzuspto-grants-1986_01
ORD IDord-10e83b837b484900854eb67bb2d5f68a
Quellennotizuspto-grants-1986_01