HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Diglycidyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (-)-Epichlorohydrin | HCID 2734062 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diglycidyl ether | HCID 16704 | — |
Reaction Steps
The starting formula derivative (2.50 g) of the following formula: ##STR17## and the same R-(-)-epichlorohydrin (4.25 g) and benzyltriethylammonium chloride (20 mg) as used in Preparation 2 are dissolved in dimethylformamide (3 ml) and thereto is added dropwise 24 wt. % aqueous sodium hydroxide (1.2 equivalent) at 60° C. After reacting at the same temperature for 40 minutes, the reaction mixture is cooled to room temperature and extracted with ether. The extract is distilled under reduced pressure to remove the solvent. The residue is purified by silica gel chromatography to give S isomer of glycidyl ether (1.62 g) of the following formula: ##STR18##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05308540 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-d636f4ac8c7a4f24aa84c88bb658e5fd |
| Source note | uspto-grants-1994_05 |