HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42757Erstellt: 24. Oktober 2026
Ethylene Glycol → 2-(3-Bromophenyl)-2-methyl-1,3-dioxolane
https://huagongshe.com/de/reaction/42757
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethylene Glycol | HCID 174 | — |
| Edukt | Nitrogen | HCID 947 | — |
| Edukt | Trimethyl orthoformate | HCID 9005 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 3'-Bromoacetophenone | HCID 16502 | — |
| Produkt | 2-(3-Bromophenyl)-2-methyl-1,3-dioxolane | HCID 10999218 | — |
Reaktionsschritte
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 1-(3-bromo-phenyl)-ethanone (1360 mg, 6.83 mmol) in ethylene glycol (8.00 mL, 143.46 mmol) was treated with trimethylorthoformate (1.50 mL, 13.68 mmol) followed by LiBF4 (131 mg, 1.37 mmol). The reaction mixture was heated at 95° C. for 15 h. Sat. aq. Na2CO3 was added and the mixture was extracted twice with ether and the combined organic extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (20:1 hept-EA) gave the title compound as a pale yellow oil: TLC:rf (10:1 hept-EA)=0.34. LC-MS-conditions 02: tR=1.01 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08536209B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-2395729cc9094f8db19164bab0b1ef65 |
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| Quellennotiz | uspto-grants-2013_09 |
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