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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679128Generated: October 26, 2026

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

https://huagongshe.com/reaction/1679128

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04079062
Source datasetuspto-grants-1978_03
ORD IDord-4c3488e9e9b24c9492349b3290d13e59
Source noteuspto-grants-1978_03