HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 1-(4-Allyloxyphenyl)-2-(4-diphenylmethylpiperazinyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(4-Diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanol | HCID 3071160 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Allyloxyphenyl)-2-(4-diphenylmethylpiperazinyl)ethanol | HCID 10320390 | 64% |
Reaction Steps
In 1.2 liters of ethanol were dissolved 120 g (0.31 mol) of 2-(4-diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)-ethanol, 74.8 g (0.62 mol) of allyl bromide and 41 g of potassium hydroxide. The resultant solution was heated with refluxing for one hour. After cooling the solution and then removing the solvent, the residue was added with 1.0 liter of ethyl acetate. The resultant mixture was washed successively with an aqueous 1N solution of sodium hydroxide, water and saturated saline, followed by drying over anhydrous sodium sulfate. The solvent was removed, and the residue was crystallized from a mixed solvent of ethanol and n-hexane to give 84.6 g of 1-(4-allyloxyphenyl)-2-(4-diphenylmethylpiperazinyl)ethanol (yield: 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04528194 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-0aac2fb3855742bda7200f6e4e9e1e46 |
| Source note | uspto-grants-1985_07 |