HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylamide → 2,2-dibutyl-4-oxo-2,3-dihydro-4H-1,3-benzoxazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylamide | HCID 5147 | — |
| Reactant | 5-Nonanone | HCID 10405 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,2-dibutyl-4-oxo-2,3-dihydro-4H-1,3-benzoxazine | HCID 10084017 | 92.5% |
Reaction Steps
A mixture of 20 g of dibutylketone, 19.3 g of salicylamide and 2.7 g of p-toluenesulfonic acid monohydrate is added to 300 ml of toluene and the mixture is refluxed overnight by making use of a dehydrator of Dean Stark. After cooling, the reaction mixture is washed, dried and evaporated to remove the solvent. The residue is purified by silica gel column chromatography (solvent; hexane:ethyl acetate=95:5) to obtain 34 g of 2,2-dibutyl-4-oxo-2,3-dihydro-4H-1,3-benzoxazine as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06011150 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-c6d2c609d24a44d1bf46a6f36adbfdfb |
| Source note | uspto-grants-2000_01 |