HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → p-Chlorophenacyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | P-Chloroacetophenone | HCID 7467 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | p-Chlorophenacyl bromide | HCID 68303 | — |
Reaction Steps
To a stirred, cooled solution of 4-chloroacetophenone (100 g, 0.65 mole), anhydrous ether (650 ml) and dioxane (325 ml) was added bromine (35 ml, 0.65 mole) dropwise over a period of 1.25 hours, keeping the temperature at 20° C. (±5° C.). The solution was then washed with water (3 × 1 l). The collected ether layer was dried over magnesium sulfate and the ether solution was evaporated under reduced pressure to give a solid. The solid was washed with water, collected by filtration, and air-dried to give the α-bromo-4-chloroacetophenone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04049650 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-675651b12dee4e628a75a408a3b2658b |
| Source note | uspto-grants-1977_09 |