HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → (4-[1,3]Dioxolan-2-yl-2-fluorophenoxy)triisopropylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-Fluoro-4-triisopropylsilanyloxybenzaldehyde | HCID 59730027 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (4-[1,3]Dioxolan-2-yl-2-fluorophenoxy)triisopropylsilane | HCID 59730094 | — |
Reaction Steps
Into a 5 L 3-neck flask equipped with a condenser and a Dean-Stark trap add 3-fluoro-4-triisopropylsilanyloxybenzaldehyde (Example 737, Part A) (90.14 g, 0.3041 mol), ethylene glycol (188.75 g, 3.041 mol), and p-toluenesulfonic acid (0.58 g, 0.003041 mol) in toluene (3.155 L). Heat to boil and reflux until 130 mL of H2O (lower layer) is collected in the Dean-Stark trap (5 hrs). Cool to room temperature, wash with 10% aqueous potassium carbonate solution (2×1 L) and brine (2×1 L), and dry over sodium sulfate. Filter and concentrate to give the crude produce.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560463B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-6ca6ef4b9649460b9f2e7bef9ab115ff |
| Source note | uspto-grants-2009_07 |