HuagongsheHuagongshe Chemistry Print Report · For research reference only
ethyl 2-(N-methyleneamino)-2-methylpropanoate → ethyl 2-[2,3-dihydro-5-(2-methoxyphenyl)-6-methyl-4-oxo-4H-1,3-oxazin-3-yl]-2-methylpropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | ethyl 2-(N-methyleneamino)-2-methylpropanoate | HCID 10855576 | — |
| Reactant | Ethyl 2-(2-methoxyphenyl)acetoacetate | HCID 22118306 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | ethyl 2-[2,3-dihydro-5-(2-methoxyphenyl)-6-methyl-4-oxo-4H-1,3-oxazin-3-yl]-2-methylpropanoate | HCID 22118261 | 117.4% |
Reaction Steps
A solution of ethyl 2-(N-methyleneamino)-2-methylpropionate (10.3 g) in xylene was added during 1 hour to a solution of ethyl 2-(2-methoxyphenyl)acetoacetate (8.51 g) in xylene whilst heating under reflux. The rate of addition was controlled so as to equal the rate of azeotropic distillation (via a Dean and Stark separator). Additional xylene was then added and distillation continued for 3 hours. The mixture was evaporated in vacuo to give ethyl 2-[2,3-dihydro-5-(2-methoxyphenyl)-6-methyl-4-oxo-4H-1,3-oxazin-3-yl]-2-methylpropanoate (14.1 g), NMR 1.25(t,3H), 1.55(s,6H), 1.8(s,3H), 3.75(s,3H), 4.1 5(m,2H), 5.3(s,2H), 6.9-7.3(m,4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06159902 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-114cbdb38a204f1e81f54d33ccd4ce04 |
| Source note | uspto-grants-2000_12 |