HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 903Erstellt: 23. Oktober 2026
Ethylene Glycol → 6-Bromo-1,4-dioxaspiro[4.6]undecane
https://huagongshe.com/de/reaction/903
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethylene Glycol | HCID 174 | — |
| Edukt | Cycloheptanone | HCID 10400 | — |
| Edukt | Bromine | HCID 24408 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 6-Bromo-1,4-dioxaspiro[4.6]undecane | HCID 288226 | — |
Reaktionsschritte
Bromine (44.8 g, 0.28 mol) was added dropwise to a stirred solution of cycloheptanone (28.5 g, 0.25 mol) in a 1:1 solution (300 mL) of ethylene glycol and tetrahydrofuran at room temperature. The mixture was stirred for 5 hours, then poured into aqueous sodium bicarbonate and extracted 3× with diethyl ether. The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo to give 2-bromocycloheptanone ethylene ketal (60 g). A mixture of this crude bromo ketal and a methanolic solution of sodium methoxide (250 mL, 25 wt. % solution) was heated at reflux overnight. The mixture was cooled to ambient temperature, poured into water, and extracted with hexanes. The organic layer was washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo to afford 2-cycloheptenone ethylene ketal (39 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05723462 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-c3c99a608b9c4984be003f74893691b4 |
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| Quellennotiz | uspto-grants-1998_03 |
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