HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 2-(Bromomethyl)-2,4-bis(4-chlorophenyl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Reactant | 1-(4-Chlorophenyl)-1,2-ethanediol | HCID 101107 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Bromomethyl)-2,4-bis(4-chlorophenyl)-1,3-dioxolane | HCID 20332620 | — |
Reaction Steps
A mixture of 11.7 parts of 2-bromo-4'-chloroacetophenone, 9 parts of 1-(p-chlorophenyl)-1,2-ethanediol, 0.5 parts of p-toluenesulfonic acid and 80 parts of benzene is stirred and refluxed for 2 days with water-separator. The reaction mixture is cooled and washed successively twice with a sodium hydrogen carbonate solution and once with water. The organic phase is dried and evaporated. The residue is triturated in petroleum ether and cooled on ice. The precipitated product is filtered off, crystallized from methanol, stirred in acetonitrile while cooling on ice, filtered off again and washed once more with acetonitrile, yielding 2-(bromomethyl)-2,4-bis(p-chlorophenyl)-1,3-dioxolane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04209447 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-700a3e22731848aeb67d8cb1901608bf |
| Source note | uspto-grants-1980_06 |