HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Benzene, (1,1-dimethylethoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | tert-Butyl peroxybenzoate | HCID 11966 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzene, (1,1-dimethylethoxy)- | HCID 81179 | — |
Reaction Steps
In this example, phenyl t-butyl ether is prepared. Grignard reagent, phenyl magnesium bromide, is formed by mixing 100 g magnesium turnings with 607.7 g bromobenzene and 6170 g anhydrus ethyl ether. After formation of the Grignard reagent, t-butyl per benzoate (449 g) in ether is added at 15° C.-25° C. under nitrogen with stirring. Reaction product is shaken with cold, dilute hydrochloric acid, then washed with dilue aqueous sodium hydroxide, and then washed with water. It is then dried and distilled to yield 269.2 G of product phenyl t-butyl ether which is analyzed to give 79.1% C (calc 80.0%) and 9.2% H (calc 9.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04244704 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-f26e7df39ddf4606b19750286726010b |
| Source note | uspto-grants-1981_01 |