Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (-)-Epichlorohydrin | HCID 2734062 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 53485842 | HCID 53485842 | 80% |
Reaction Steps
Into a reaction vessel were put phthalimide (2.00 g, 13.6 mol), (R)-epichlorohydrin (2.26 g, 24.5 mmol), anhydrous sodium carbonate (0.72 g, 6.80 mmol), tetra n-butylammonium hydrogensulfate (0.46 g, 1.36 mol) and isopropanol (13 ml) and the mixture was reacted at room temperature at 50° C. for 23 hours. And then to the residue was gradually added potassium tert-butoxide (1.83 g, 16.3 mmol) in isopropanol and the mixture is stirred at 20° C. for 1 hour. After the reaction, post-treatment was carried out to give crude (R)-glycidylphthalimide (2.21 g, yield 80%, optical purity 98% e.e.) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135576B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-fe10052bf4ce428da9890054ec050eb0 |
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| Source note | uspto-grants-2006_11 |
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