HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-(4,4-Diethoxy-butoxy)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 4-Chlorobutyraldehyde Diethyl Acetal | HCID 262598 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | 2-(4,4-Diethoxy-butoxy)ethanol | HCID 23090643 | — |
Reaction Steps
A mixture of anhydrous ethylene glycol (120 g, 1.93 moles), a 1.0M solution of potassium tert-butoxide in tert-butanol (70 ml, 0.07 moles), and 4-chlorobutyraldehyde diethyl acetal (11 g, 0.061 moles) is stirred overnight at 100° C. under an argon atmosphere. After cooling to room temperature, the reaction mixture is added to 600 ml distilled water. The product is extracted with dichloromethane (150, 125, and 125 ml). The combined extracts are then dried with anhydrous magnesium sulfate and the solvent is distilled off under reduced pressure. Next the product is subjected to vacuum distillation (kugelrohr, t=90-110° C., 0.10 mm Hg). Yield 5.5 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076412B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-925c66e6cea8476f9998c6b5a0ec55aa |
| Source note | uspto-grants-2011_12 |