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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
Edukt1-ButanolHCID 263—
Eduktp-Toluenesulfonic acidHCID 6101—
Edukt2-Bromo-2'-acetonaphthoneHCID 69179—
LösungsmittelEthylene GlycolHCID 174—
Produkt1,3-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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04079062
Quelldatensatzuspto-grants-1978_03
ORD IDord-4c3488e9e9b24c9492349b3290d13e59
Quellennotizuspto-grants-1978_03