HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1679128Erstellt: 26. Oktober 2026
Benzene → 1,3-Dioxolane, 2-(bromomethyl)-2-(2-naphthalenyl)-
https://huagongshe.com/reaction/1679128
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzene | HCID 241 | — |
| Edukt | 1-Butanol | HCID 263 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 2-Bromo-2'-acetonaphthone | HCID 69179 | — |
| Lösungsmittel | Ethylene Glycol | HCID 174 | — |
| Produkt | 1,3-Dioxolane, 2-(bromomethyl)-2-(2-naphthalenyl)- | HCID 607997 | — |
Reaktionsschritte
To a stirred solution of 74.4 parts of 2-bromo-1-(2-naphthalenyl)-1-ethanone in 240 parts of a butanol are added successively 3 parts of 4-methylbenzenesulfonic acid and 270 parts of benzene. Then there are added dropwise 28 parts of 1,2-ethanediol. Upon completion, stirring is continued overnight at reflux temperature. The reaction mixture is evaporated. The residue is dissolved in 2,2'-oxybispropane and the solution is stirred with a diluted sodium hydroxide solution. The layers are separated and the aqueous phase is extracted with 2,2'-oxybispropane. The extra ct is neutralized with water, dried, filtered and evaporated. The oily residue is crystallized from methanol. The product is filtered off and recrystallized from methanol, yielding 41 parts of 2-(bromomethyl)-2-(2-naphthalenyl)-1,3-dioxolane; mp. 64° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04079062 |
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| Quelldatensatz | uspto-grants-1978_03 |
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| ORD ID | ord-4c3488e9e9b24c9492349b3290d13e59 |
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| Quellennotiz | uspto-grants-1978_03 |
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