HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 24752052, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 1,2-Diaminocyclohexane, trans- | HCID 43806 | — |
| Reactant | 3,4-Difluorobenzaldehyde | HCID 588088 | — |
| Product | HCID 24752052 | HCID 24752052 | — |
Reaction Steps
The title compound was prepared from (±)-trans-1,2-cyclohexanediamine and 3,4-difluorobenzaldehyde by Procedure C. After reacting with cyanogen bromide, the reaction mixture was evaporated to dryness and the crude product washed with ether and recrystallized from MeOH to give the title compound as the hydrogen bromide salt (mp 238-240° C.). MS (ES+) m/z 392 ([M+1]+, 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048877B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-e83eb20cb7d14388bd92d7273355ee1f |
| Source note | uspto-grants-2011_11 |