HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 3-benzyloxycarbonylamino-6-methyl-2-pyridinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 178425908 | HCID 178425908 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-benzyloxycarbonylamino-6-methyl-2-pyridinone | HCID 10083840 | — |
Reaction Steps
Diphenylphosphoryl azide (11.9 mL, 55 mmol) was added to a solution of 2-hydroxy-6-methylpyridine-3-carboxylic acid (7.65 g, 50 mmol) and triethylamine (7.7 mL, 55 mmol) in dry dioxane (100 mL) and the resulting solution was heated to reflux. After 16 h additional triethylamine (7.7 mL, 55 mmol) and benzyl alcohol (5.7 mL, 50 mmol) were added and the solution was refluxed for a further 24 h. The reaction mixture was concentrated in vacuo and the residue was partitioned between methylene chloride (200 mL) and brine (100 mL), and acidified to pH 1 with 10% HCl. The organic layer was washed with saturated NaHCO3 (2×100 mL), brine (100 mL), dried over Na2SO4, and filtered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06420397B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-2180bd3fac2a4ff9a1e0b4ee4aa998ed |
| Source note | uspto-grants-2002_07 |