HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → 4-Chloro-2-methoxyphenyl-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(4-Chloro-2-methoxyphenyl)ethan-1-one | HCID 19429468 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-2-methoxyphenyl-1,3-dioxolane | HCID 86735530 | — |
Reaction Steps
To a stirred solution of 27.5 parts of 1-(4-chloro-2-methoxyphenyl)ethanone in 160 parts of butanol are added dropwise 24 parts of bromine. After stirring for 1 hour at room temperature, there are added successively 9.3 parts of 1,2-ethanediol, 3 parts of 4-methylbenzenesulfonic acid and 450 parts of benzene. Stirring is continued overnight at reflux temperature with water-separator. The reaction mixture is evaporated and the residue is taken up in benzene. The mixture is washed with a diluted sodium hydroxide solution and three times with water, dried, filtered and evaporated. The residue is crystallized from methanol, yielding 27.6 parts (60%) of 2-(bromomethyl)-2-(4-chloro-2-methoxyphenyl-1,3-dioxolane; mp. 110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04079062 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-5e7ed5dafbde4c9db0eced5c397a45a8 |
| Source note | uspto-grants-1978_03 |