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 | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53485842 | HCID 53485842 | 82% |
Reaction Steps
Into a reaction vessel were put potassium phthalimide (5.00 g, 27.0 mmol), benzyltrimethylammonium chloride (0.50 g, 2.70 mmol) and DMF (50 ml) and then thereto was added (R)-epichlorohydrin (5.00 g, 54.0 mmol). The mixture was stirred at room temperature for 16 hours and the solvent was removed. To the residue was added ethyl acetate (30 ml), the mixture was washed with water (20 ml) and ethyl acetate was removed to give crude (R)-glycidylphthalimide (4.48 g, yield: 82%, optical purity: 63% e.e.) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135576B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-c8ab02ddd9c942c7a20200dba28baf31 |
| Source note | uspto-grants-2006_11 |