HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrafluoroboric acid → 1-Bromo-4-fluoro-2,5-dimethylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | 4-Bromo-2,5-dimethylaniline | HCID 8167130 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Bromo-4-fluoro-2,5-dimethylbenzene | HCID 13553414 | — |
Reaction Steps
373 g of 2-amino-5-bromo-p-xylene were suspended in 1860 ml of H2O in a 4 l four-necked flask, the mixture was cooled to 3° C. (internal temperature), and 612 ml of tetrafluoroboric acid were added. 154 g of NaNO2 in 300 ml of water were then added dropwise over the course of 60 minutes. After 60 minutes, the solid was filtered off with suction and washed with a little cold 5% tetrafluoroboric acid, then with a little cold methanol and finally with a little cold diethyl ether. The yellow solid (497 g=90%) was dried overnight in an oil-pump vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06638646B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-e51053d09f1b4274b143001d3f3e033a |
| Source note | uspto-grants-2003_10 |