HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-(3-nitrophenyl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Benzene | HCID 241 | — |
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(3-nitrophenyl)-1,3-dioxolane | HCID 240610 | 101.2% |
Reaction Steps
A mixture of 3-nitrobenzaldehyde (100 g, 0.66 mole), ethylene glycol (49.3 g, 0.7 mole) and p-toluenesulfonic acid (0.8 g) and benzene (1 L) was heated at reflux with continuous removal of water via a Dean and Stark trap. After 4 hours, the mixture was cooled, filtered through a pad of neutral alumina and concentrated in vacuo to afford 2-(3-nitrophenyl)-1,3-dioxolane (130.4 g, 100%) as an amber oil used without further purification below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04701459 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-5b4ac652bfc34523811da326226c9728 |
| Source note | uspto-grants-1987_10 |