HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 2-(Bromomethyl)-4-[(4-chlorophenoxy)methyl]-2-(4-chlorophenyl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Chlorphenesin | HCID 7697 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(Bromomethyl)-4-[(4-chlorophenoxy)methyl]-2-(4-chlorophenyl)-1,3-dioxolane | HCID 20332649 | — |
Reaction Steps
A mixture of 11.7 parts of 2-bromo-4'-chloroacetophenone, 12.2 parts of 1-(p-chlorophenoxy)-2,3-propanediol, 3 parts of p-toluenesulfonic acid and 240 parts of benzene is stirred and refluxed for 20 hours in a four-necked round-bottom flask equipped with a watertrap. The benzene solution is washed successively with a diluted sodium hydroxide solution and with water. The solvent is removed in vacuo. The residue is triturated in methanol. The precipitated product is filtered off (methanol filtrate is set aside) and crystallized from toluene, yielding A-2-(bromomethyl-4-(p-chlorophenoxymethyl)-2-(p-chlorophenyl)-1,3-dioxolane; m.p. 165°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03936470 |
| Source dataset | uspto-grants-1976_02 |
| ORD ID | ord-ed4f67585ce84caeb44a058025c132e3 |
| Source note | uspto-grants-1976_02 |