HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzhydrol → HCID 19850789, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzhydrol | HCID 7037 | — |
| Reactant | HCID 19850790 | HCID 19850790 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 19850789 | HCID 19850789 | — |
Reaction Steps
10.1 g of benzhydrol are refluxed with 6.2 g of potassium tertiary butoxide in 100 ml of anhydrous tertiary butanol under argon gas for 30 minutes, then 19.6 g of 1-[3-[(4-fluorophenyl)-phenylmethoxy]propyl]-4-(2-chloroethyl)piperazine dissolved in 40 ml of anhydrous tertiary butanol are dropwise added. The mixture is boiled for one additional hour, then evaporated to about 40 ml under reduced pressure and after adding water it is extracted with benzene. The organic phase is dried over anhydrous magnesium sulfate and, after evaporating benzene under reduced pressure, the residue is fractionally distilled. The aimed compound boils at 247°-250° C./0.01 Hgmm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04866062 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-b51c3398b23e4eb7b67e014885afa270 |
| Source note | uspto-grants-1989_09 |