HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 4-Bromo-3-(1,3-dioxolan-2-yl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | 2-Bromo-5-hydroxybenzaldehyde | HCID 387179 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Catalyst | Potassium Carbonate | HCID 11430 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Bromo-3-(1,3-dioxolan-2-yl)phenol | HCID 57968707 | 90.2% |
Reaction Steps
A mixture of 2-bromo-5-hydroxybenzaldehyde (60.0 g, 299 mmol), ethylene glycol (56 mL, 1.00 mol), and p-toluenesulfonic acid (1.14 g, 5.98 mmol) in toluene (450 mL) was refluxed with Dean-Stark head for overnight. Potassium carbonate (3 g) was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried on anhydrous sodium sulfate. The solvent was removed under reduced pressure to give 4-bromo-3-(1,3-dioxolan-2-yl)phenol (66.1 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461135B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-1b6bb8887fac4b3ebbdc6ef8b1500897 |
| Source note | uspto-grants-2013_06 |