HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylene Glycol → 2-[2-(2-Propoxyethoxy)ethoxy]ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylene Glycol | HCID 8172 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromopropanol | HCID 12887879 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[2-(2-Propoxyethoxy)ethoxy]ethanol | HCID 11355992 | 18% |
Reaction Steps
Triethylene glycol (19.5 g, 0.13 mol) was dissolved in tetrahydrofuran (150 mL) and sodium hydride (2.60 g, 0.065 mol) was added portion wise over 0.5 h and the reaction was stirred for an additional 1 h. Then 1-bromopropanol (8.0 g, 0.065 mol) dissolved in tetrahydrofuran (30 mL) was added dropwise via addition funnel and the reaction was stirred overnight at room temperature. Crude reaction mixture was filtered through Celite, washed CH2Cl2, and evaporated to dryness. The resultant oil was dissolved in CH2Cl2 (250 mL), washed sat. NaCl (250 mL), H2O (250 mL), dried MgSO4, and evaporated to dryness. Column chromatography (Silica, ethyl acetate) afforded 1 a yellowish oil (2.24 g, 18% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08563685B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-54b5372ef85b4c41b6dc99e8933e2e88 |
| Source note | uspto-grants-2013_10 |