HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetone → 3-Phenyl-6-(m-chlorophenyl)-5-hexen-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetone | HCID 7678 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | m-Chlorocinnamyl bromide | HCID 54032824 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 3-Phenyl-6-(m-chlorophenyl)-5-hexen-2-one | HCID 53705377 | — |
Reaction Steps
Sodium hydride (25.20 g., 0.60 mole, oil dispersion) is suspended in glyme (800 ml.) and phenyl acetone (80.50 g., 0.60 mole) in glyme (100 ml.) is added dropwise with stirring. After complete addition the mixture is heated to reflux for one hour. The mixture is cooled to room temperature and a solution of crude m-chlorocinnamyl bromide (139 g., 0.6 mole) in glyme (100 ml.) is added dropwise. When addition is complete the mixture is refluxed for 24 hours then allowed to cool. After filtration of inorganic salts and removal of solvent from the filtrate, vacuum distillation provides 36.11 g., b.p. 158.5°-163°/0.1 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03956374 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-84d02f43db0a4194a5d81565a0c94a27 |
| Source note | uspto-grants-1976_05 |