HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 1,3-Dioxolane, 2-(3-bromo-4-fluorophenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 3-Bromo-4-fluorobenzaldehyde | HCID 173604 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,3-Dioxolane, 2-(3-bromo-4-fluorophenyl)- | HCID 10977765 | 85% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
26 g (0.24 mol) of trimethylchlorosilane were added to a mixture of 20.3 g (0.1 mol) of 3-bromo-4-fluoro-benzaldehyde and 6.8 g (0.11 mol) of ethane-1,2-diol and the mixture was heated to 100° C. for 3 hours. After cooling to room temperature, 100 ml of toluene were added and the mixture was shaken twice with 50 ml of ice-water each time. The organic phase was dried over sodium sulphate and evaporated in vacuo. The residue was distilled in vacuo. 21 g (85% of theory) of 3-bromo-4-fluoro-benzaldehyde ethyleneacetal were thus obtained in the form of a colorless oil with a boiling point of 79°-81° C./0.1 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04626601 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-80b5c38787e348e0bea92c8485b782a7 |
| Source note | uspto-grants-1986_12 |