HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Octanol → Diglycidyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Octanol | HCID 957 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Product | Diglycidyl ether | HCID 16704 | — |
Reaction Steps
Octanol (132 g, 1 mol) was added to a round-bottomed four-neck flask equipped with an agitator, reflux condenser and thermometer at 30° C. Tetrabutylammonium bromide (16.1 g, 0.050 mol) and sodium hydroxide (61.9 g, 1.5 mol) were further added to the flask and stirred, and then, epichlorohydrin (140.1 g, 1.5 mol) was added dropwise for 10 minutes. After the mixture was stirred for 3 hours at the same temperature, by-products such as sodium chloride and sodium hydroxide were filtered off. The unreacted epichlorohydrin was reused via recovery process such as distillation. Then, glycidyl ether compound as the desired product was obtained by a simple filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06392064B2 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-27adc02a10b84d49a157a5affbb85927 |
| Source note | uspto-grants-2002_05 |