Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | HCID 54021829 | HCID 54021829 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 54122965 | HCID 54122965 | 85.5% |
Reaction Steps
Fifty grams (0.15 mol) of 4-hydroxy-3,5-dimethyl-β,β-diphenylpropiophenone (prepared as in Example 5), dissolved in 200 mls of acetone, are added, with stirring, to a reaction mixture consisting of 29 grams (0.184 mol) of 1-bromo-3-chloropropane in 300 mls of acetone and 42 grams (0.304 mol) of water-free potash. The preparation is boiled under reflux for one day and the precipitate is sucked off. The acetone is evaporated, the residue taken up with ether and a little acetone and, subsequently, washed with water. The ethereal phase is dried over sodium sulfate. The solvent is evaporated in vacuo. The residue is crystallized from acetone/petroleum ether. Fifty-two and five-tenths grams [85.5%] of 4-(3-bromopropoxy)-3,5-dimethyl-β,β-diphenylpropiophenone are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04140770 |
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| Source dataset | uspto-grants-1979_02 |
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| ORD ID | ord-b7be2de0cced49b99745cf94a87b348a |
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| Source note | uspto-grants-1979_02 |
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