HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sulfuryl chloride → 1H-Isoindole-1,3(2H)-dione, 2-(4-chloro-2-fluoro-5-(1-methylethoxy)phenyl)-4,5,6,7-tetrahydro-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sulfuryl chloride | HCID 24648 | — |
| Edukt | N-(2-Fluoro-5-isopropoxyphenyl)-3,4,5,6-tetrahydrophthalimide | HCID 13556385 | — |
| Katalysator | Dicyclohexylamine | HCID 7582 | — |
| Lösungsmittel | Tetrachloroethylene | HCID 31373 | — |
| Produkt | 1H-Isoindole-1,3(2H)-dione, 2-(4-chloro-2-fluoro-5-(1-methylethoxy)phenyl)-4,5,6,7-tetrahydro- | HCID 158650 | 83,1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04563535 |
| Quelldatensatz | uspto-grants-1986_01 |
| ORD ID | ord-10e83b837b484900854eb67bb2d5f68a |
| Quellennotiz | uspto-grants-1986_01 |