Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 18795541 | HCID 18795541 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 18795525 | HCID 18795525 | 21.5% |
Reaction Steps
N-Iodosuccinimide (238 g) was added to a stirred solution of ethyl 2-(2,3-dihydro-6-methyl-4-oxo-4H-1,3-oxazin-3-yl)-2-methylpropanoate (200 g) in acetic acid. The mixture was stirred at 40-45° C. for 5 hours then at ambient temperature overnight and evaporated. The residue was diluted with ether, washed with water, sodium carbonate solution (2M) and brine, dried (MgSO4) and evaporated. A solution of the residue in ethanol was cooled to -40° C. to give ethyl 2-(2,3-dihydro-5-iodo-6-methyl-4-oxo-4H-1,3-oxazin-3-yl)-2-methylpropanoate (66.9 g), m.p. 85-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06046135 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-7b295aee12a64fccb0c23c8865aeff02 |
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| Source note | uspto-grants-2000_04 |
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