Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Tetraethylene Glycol | HCID 8200 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | 3,6,9,12-Tetraoxaeicosan-1-ol | HCID 5414 | — |
Reaction Steps
Tetraethyleneglycol (1243 g, 6.40 mol) was heated at 100° C. for 30 minutes with stirring and vigorous N2 bubbling, then cooled to 60° C. A 50% NaOH solution (70.4 g, 0.88 mol) was added and the resulting solution was heated at 100°-105° C. for 30 minutes with N2 bubbling. The solution was cooled to 60° C., bromooctane (154 g, 0.80 mol) was added, and the reaction was heated at 100°-110° C. for 24 hours. The reaction solution was cooled, added to ice water and extracted twice with methylene chloride. The combined extracts were washed with 10% NaOH, water and brine; dried, treated with charcoal, and filtered through a thin silica gel pad. The solvent was removed in vacuo; the residual product (155 g, 63%) was a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04988604 |
|---|
| Source dataset | uspto-grants-1991_01 |
|---|
| ORD ID | ord-ac3b16678f6c49a0b2eeeca8d862309d |
|---|
| Source note | uspto-grants-1991_01 |
|---|