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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971635Generated: October 27, 2026

Benzene → 1,3-Dioxolane, 2-(bromomethyl)-2-(2-naphthalenyl)-

https://huagongshe.com/reaction/971635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant1-ButanolHCID 263—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-Bromo-2'-acetonaphthoneHCID 69179—
SolventEthylene GlycolHCID 174—
Product1,3-Dioxolane, 2-(bromomethyl)-2-(2-naphthalenyl)-HCID 607997—

Reaction Steps

To a stirred solution of 74.4 parts of 2-bromo-1-(2-naphthalenyl)-1-ethanone in 240 parts of 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 extract 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04160838
Source datasetuspto-grants-1979_07
ORD IDord-0c516d00863c46ada44e4db8fd091834
Source noteuspto-grants-1979_07