HuagongsheHuagongshe Chemistry Print Report · For research reference only
(-)-Epichlorohydrin → HCID 53485842, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (-)-Epichlorohydrin | HCID 2734062 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Catalyst | Benzyltrimethylammonium chloride | HCID 5963 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 53485842 | HCID 53485842 | 83.1% |
Reaction Steps
Into a reaction vessel were put potassium phthalimide (50.0 g, 0.27 mol), benzyltrimethylammonium chloride 5.00 g, 0.027 mol) and isopropanol (500 ml), and the mixture was cooled to 10° C. Thereto was added (R)-epichlorohydrin (74.9 g, 0.81 mol) and the mixture was stirred for 46 hours while being cooled. The solvent was removed and to the residue was added ethyl acetate (250 ml). The mixture was washed with water (250 ml), and then ethyl acetate was removed to give crude (R)-glycidylphthalimide (optical purity: 97% e.e.). The crude product was crystallized from ethyl acetate-hexane to give the object (R)-glycidylphthalimide (45.6 g, yield: 83%, optical purity: 98% e.e.) as white crystals. mp 100-102° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06875875B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-321adb9ac48342109080399537092360 |
| Source note | uspto-grants-2005_04 |