HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234903Generated: October 25, 2026
Water → 2-butyl-7-methoxycarbonyl-4-(2-propyl)-3-oxo-3,4-dihydro-2H-1,4-benzoxazine
https://huagongshe.com/reaction/234903
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-butyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine | HCID 10539473 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-butyl-7-methoxycarbonyl-4-(2-propyl)-3-oxo-3,4-dihydro-2H-1,4-benzoxazine | HCID 10686018 | 21.1% |
Reaction Steps
To a solution of 2 -butyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (9.0 g) in dimethylformamide (180 ml) were added 60% sodium hydride (in oil) (1.63 g) and 2-iodopropane (6.35 g) and the mixture was stirred at 80° C. for 2 hours. Water was added to the reaction solution and extraction with ethyl acetate was conducted. The solvent was distilled off under reduced pressure and the resulting residue was subjected to purification by column chromatography using ethyl acetate/hexane [1:8 (v/v)] to give 2-butyl-7-methoxycarbonyl-4-(2-propyl)-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (2.2 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05597820 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-f5a0dc03586e452d89f768697f7cbfbe |
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| Source note | uspto-grants-1997_01 |
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