HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → 4-(3-chloro-2-hydroxypropylamino)-N-methylphthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | 5-amino-2-methyl-2,3-dihydro-1H-isoindole-1,3-dione | HCID 726931 | — |
| Solvent | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Product | 4-(3-chloro-2-hydroxypropylamino)-N-methylphthalimide | HCID 21281736 | 77.3% |
Reaction Steps
Twenty-five grams (g) (0.142 mole) 4-amino-N-methylphthalimide [Flitsch, Chem. Ber. 94:2494(1961)] and 20.7 g (0.21 mole) 1-chloro-2,3-epoxypropane were added to 150 ml 2,2,2-trifluoroethanol and the reaction mixture was heated to reflux with stirring for 48 hours. Seventy to eighty ml of 2,2,2-trifluoroethanol was removed by distillation and a heavy yellow precipitate formed when the remaining solution cooled to room temperature. This precipitate was triturated with ethyl acetate, collected by filtration and dried to give 29.5 g (77% yield) of the desired phthalimide intermediate m.p. 136°-138.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04363759 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-af7f62e27b714720a4f472f3c5901a3a |
| Source note | uspto-grants-1982_12 |