HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromoaniline → HCID 11811432, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 11129151 | HCID 11129151 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11811432 | HCID 11811432 | 75.8% |
Reaction Steps
A mixture of 1.9 g (7.6 mmol) of 4-chloro-8-methoxy-6-nitro-quinoline-3-carbonitrile and 0.86 ml (8.3 mmol) of 3-bromo aniline in 95 ml ethanol was refluxed under nitrogen for 5 hours. The reaction mixture was poured into diluted sodium bicarbonate solution. Ethanol was removed under vacuum. The mixture was diluted with ethyl acetate and the organic layer was separated and dried over sodium chloride. The solution was concentrated and solid was collected and then washed with hexane. Upon drying, 2.3 g of yellow solid obtained: mass spectrum (electrospray, m/e) M+H 398.8 and 400.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE042376E1 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-f1a654fc4c2a43d797a012b3a8b8a1d8 |
| Source note | uspto-grants-2011_05 |