HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → (2R)-2-(Phenoxymethyl)oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (+)-Epichlorohydrin | HCID 149428 | — |
| Catalyst | Benzyltrimethylammonium chloride | HCID 5963 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2R)-2-(Phenoxymethyl)oxirane | HCID 1534344 | 80% |
Reaction Steps
To a reaction vessel were added (S)-epichlorohydrin (99% ee, 2.64 g, 29 mmol), benzyltrimethylammonium chloride (36 mg), 1,2-dichloroethane (6 ml) and water (6 ml), and the mixture was cooled with ice. After addition of phenol (1.78 g, 19 mmol), thereto 24% aqueous NaOH solution (4.10 g, 25 mmol) was dropped in a ten minute period under stirring. The mixture was stirred for 30 minutes under ice-cooling and then for 42 hours at room temperature. After the aqueous layer was removed, the organic layer was neutralized with 5% HCl and washed with water twice. The solvent was removed to give objective crude (R)-glycidylphenyl ether (2.27 g, yield 80%, optical purity 98% ee) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07265232B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-3791f899e0b54655994e417b1027772e |
| Source note | uspto-grants-2007_09 |