HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 22767870, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22767875 | HCID 22767875 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 22767870 | HCID 22767870 | — |
Reaction Steps
11.9 G. of 1-[3-chloro-7-trifluoromethyl-dibenz[b,f]oxepin-10-yl]-4 -methyl-piperazine was reduced with sodium borohydride in glacial acetic acid in a manner analogous to that described in Example 14, and there is obtained crude 1-[3-chloro-10,11-dihydro-7-trifluoromethyl-dibenz[b,f]oxepin-10-yl]-4-methyl-piperazine which is recrystallized from isopropanol and melts at 110° C. The dihydrochloride, prepared in ethanol, melts at 219°-222° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04032525 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-27eb2f32d6fe459a9bc59e9d3a39bed0 |
| Source note | uspto-grants-1977_06 |