HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromodiphenylmethane → HCID 19849748, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Reactant | HCID 19849737 | HCID 19849737 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19849748 | HCID 19849748 | — |
Reaction Steps
A mixture containing 7.4 g of benzhydryl bromide and 21.8 g of 4-[(2-chlorophenyl)-(4-fluorophenyl)methyl]-1-(3-hydroxypropyl)piperazine is heated at 160° to 170° C. under nitrogen gas for 30 minutes, then cooled to 90° to 100° C. and poured into water. The aqueous phase is extracted with benzene, washed with water, thebenzene solution is dried over anhydrous potassium carbonate and then evaporated under reduced pressure. The residue is purified by chromatography on a Kieselgel column by using a 4:1 mixture of benzene andchloroform as eluant. The thus-obtained product is recrystallized from n-hexane to give the aimed product, m.p.: 98°-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04868184 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-ba2259434f744a42a0ca769c83f119d9 |
| Source note | uspto-grants-1989_09 |