HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725752Generated: October 29, 2026
Hydrochloric Acid → 2-Bromo-6-chloro-4-methylpyridine
https://huagongshe.com/reaction/725752
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Bromo-4-methylpyridin-2-amine | HCID 22176507 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-6-chloro-4-methylpyridine | HCID 11117234 | 40% |
Reaction Steps
A solution of 56 g 6-amino-2-bromo-4-methylpyridine in 500 ml of concentrated hydrochloric acid was cooled to -50° C. and saturated with gaseous HCl via a gas inlet. Under continuous cooling a solution of 25 g sodium nitrite in 60 ml water was added slowly. The reaction mixture was stirred for a further 2 hours at -50° C. The mixture was allowed to warm up to ambient temperature and set alkaline with a 50% aqueous solution of sodium hydroxide. The aqueous phase was extracted three times each with 200 ml dichloromethane. The combined extracts were dried with calcium chloride, and the solvent removed in vacuo to afford 22.5 g (40%) of 2-bromo-6-chloro-4-methylpyridine as a pale brown solid of melting point 76° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05707933 |
|---|
| Source dataset | uspto-grants-1998_01 |
|---|
| ORD ID | ord-5e06711e87bd4292b401a7e8254aeea6 |
|---|
| Source note | uspto-grants-1998_01 |
|---|