HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-(4-Bromophenyl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(4-Bromophenyl)-1,3-dioxolane | HCID 2773842 | 23,613.199% |
Reaction Steps
A solution of 4-bromobenzaldehyde (5 g, 0.027 mol), ethylene glycol (7.0 g, 0.11 mmol), and p-toluenesulfonic acid (0.1 g, 0.5 mmol) in benzene was heated at reflux for 24 h using a Dean-Stark setup to remove water. The reaction was taken up in diethyl ether (100 mL) and washed with water (5×30 mL) and brine (30 mL). The organic phase was dried over magnesium sulfate and concentrated under vacuum to afford 2-(4′-bromophenyl)-1,3-dioxolane (5.95 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06268513B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-608781426b45460a933b29f9937cb07c |
| Source note | uspto-grants-2001_07 |