HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017474Generated: October 31, 2026
Ammonium Chloride → 6-chloro-N-methyl-4-o-tolyl-nicotinamide
https://huagongshe.com/reaction/1017474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 6-Chloro-N-methylnicotinamide | HCID 12364230 | — |
| Reactant | HCID 178424304 | HCID 178424304 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-chloro-N-methyl-4-o-tolyl-nicotinamide | HCID 12167312 | 78.9% |
Reaction Steps
A solution of 1.5 g (8.8 mmol) 6-chloro-N-methyl-nicotinamide in 18 ml THF was added at 4° C. over 15 min to a solution of 21.9 ml (21.9 mmol) o-tolylmagnesium chloride 1M in THF. The reaction mixture was stirred at r.t. for 2 h cooled to 4° C. and treated dropwise over 10 min with 30.0 ml 5% aqueous NH4Cl. The aqueous phase was separated and extracted twice with THF and the organic phases were washed twice with 5% aqueous NH4Cl. The combined organic phases were dried over Na2SO4 and subsequently treated at r.t. in four portions over 10 h with 0.9 g (5.7 mmol) KMnO4. The reaction mixture was stirred for 5.5 h at r.t., filtrated and the solvent was removed. The residue was purified by chromatography over silica gel (CHCl3) to yield 1.8 g (78.9%) product as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06479483B2 |
|---|
| Source dataset | uspto-grants-2002_11 |
|---|
| ORD ID | ord-dca3e1af210b42c28562fc4fe4d1b811 |
|---|
| Source note | uspto-grants-2002_11 |
|---|