HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720748Generated: October 30, 2026
(+)-Epichlorohydrin → HCID 11608126, compound
https://huagongshe.com/reaction/720748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (+)-Epichlorohydrin | HCID 149428 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Catalyst | Benzyltrimethylammonium chloride | HCID 5963 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 11608126 | HCID 11608126 | 72% |
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 tert-buyl alcohol (50 ml) and then thereto was added (S)-epichlorohydrin (6.53 g, 54.0 mmol). The mixture was stirred at 20° C. for 24 hours and the solvent was removed. To the residue was added ethyl acetate (30 ml), the mixture was washed with water (20 ml), and then ethyl acetate was removed to give crude (S)-glycidylphthalimide (3.95 g, yield: 72%, optical purity: 97% e.e.) as a white solid.
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-57ebbce2264c4bb6b77ea4beb7739163 |
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| Source note | uspto-grants-2006_11 |
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