HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231319Generated: October 25, 2026
Ethylene Glycol → 1,3-Dioxolane, 2-(3-bromo-4-fluorophenyl)-
https://huagongshe.com/reaction/231319
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 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 |
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| Patent number | US04845249 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-98297bcf8e2744568f315cd85bcab725 |
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| Source note | uspto-grants-1989_07 |
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