Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553407Generated: October 31, 2026

Cyanogen Bromide → HCID 24752052, compound

https://huagongshe.com/reaction/553407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
Reactant3,4-DifluorobenzaldehydeHCID 588088—
ProductHCID 24752052HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048877B2
Source datasetuspto-grants-2011_11
ORD IDord-e83eb20cb7d14388bd92d7273355ee1f
Source noteuspto-grants-2011_11