HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719191Generated: October 30, 2026
Bromoacetonitrile → HCID 10157757, compound
https://huagongshe.com/reaction/719191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178483817 | HCID 178483817 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10157757 | HCID 10157757 | — |
Reaction Steps
To a suspension of 4-hydroxy-benzo[a]phenazine-11-carboxylic acid (2-dimethylamino-ethyl)-amide: hydrobromide salt (230 mg) in dry N,N-dimethylformamide (3 mL) was added potassium tert-butoxide (175 mg) and then bromoacetonitrile (47 μL). The reaction mixture was heated to 100° C. for 1 hour. The reaction mixture was then cooled, diluted with ethyl acetate, washed with sodium carbonate solution and brine, dried (MgSO4) and the solvent removed in vacuo to provide crude product. This was purified using flash chromatography (silica, 25% MeOH in ethyl acetate) to yield the title compound as a yellow solid (74 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07132419B2 |
|---|
| Source dataset | uspto-grants-2006_11 |
|---|
| ORD ID | ord-89a7693c2e8348218db6817249217a0a |
|---|
| Source note | uspto-grants-2006_11 |
|---|