HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Phenylacetophenone → 2-Bromo-1,2-diphenylethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Phenylacetophenone | HCID 9948 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Bromo-1,2-diphenylethan-1-one | HCID 102630 | 99.6% |
Reaction Steps
196 g (1 mole) of phenyl benzyl ketone were suspended in 1 liter of carbon tetrachloride. A solution of 51 ml (1 mole) of bromine in 50 ml of carbon tetrachloride were added dropwise, under irradiation (UV), at a rate such that a steady consumption of bromine took place. The solvent was then distilled off in a water pump vacuum. 274 g (quantitative yield) of ω-bromo-ω-phenyl-acetophenone of melting point 48°-50° C. were obtained. ##STR29##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04772623 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-4551e318311d4930acd224e97b3e6368 |
| Source note | uspto-grants-1988_09 |