HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 23046046, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(2-Methoxyethoxy)benzhydrol | HCID 23046047 | — |
| Reactant | 4-(2-Methoxyethoxy)benzophenone | HCID 23046051 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 23046046 | HCID 23046046 | — |
Reaction Steps
For the preparation of the compound of Example 27, 4-(2-methoxyethoxy)benzophenone is obtained by reaction of 4-hydroxybenzophenone with 2-methoxyethyl chloride at 100° C. in the presence of sodium hydride in dimethylformamide. Further reaction takes place in accordance with Example 1-5. 4-(2-Methoxyethoxy)benzophenone is reduced to 4-(2-methoxyethoxy)benzhydrol using sodium borohydride. 4-(2-Methoxyethoxy)benzhydrol is reacted with thionyl chloride in chloroform to give 4-(2-methoxyethoxy)benzhydryl chloride. 4-(2-methoxyethoxy)benzhydryl chloride is reacted with piperazine in dimethylformamide in the presence of potassium carbonate to give 1-((4-(2-methoxyethoxy)phenyl)phenylmethyl)piperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04935414 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-6a68a339f3e449468d946b6009c57a74 |
| Source note | uspto-grants-1990_06 |