Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Octanol | HCID 957 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Boron | HCID 5462311 | — |
| Product | Glycidyl n-octyl ether | HCID 92955 | 111.8% |
Reaction Steps
Octanol (130 g) and 2.84 g of a boron trifluorideether complex were cooled to 0° C. while stirring. At a temperature maintained at 0° C., 138.8 g of epichlorohydrin was added dropwise over 1 hour. After completion of dropwise addition, an excess alcohol was distilled off at 100° C. under reduced pressure (13 to 26 Pa). The reaction mixture was cooled to 50° C. and while maintaining the temperature at 50° C., 125 g of a 48% aqueous solution of sodium hydroxide was added dropwise over 1 hour. After stirring for 3 hours, 200 mL of water was added to the reaction mixture to cause separation. The water layer thus obtained was removed and then the residue was washed twice with 100 mL of water, whereby 208 g of crude octyl glycidyl ether was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06437196B1 |
|---|
| Source dataset | uspto-grants-2002_08 |
|---|
| ORD ID | ord-1d6273ad3b1349c3b3cc5b157232fe13 |
|---|
| Source note | uspto-grants-2002_08 |
|---|