HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378773Generated: October 27, 2026
3,3-Dimethyl-1,2,3,4-tetrahydroquinoxalin-2-one → 3,3-Dimethyl-4-[(1-methyl)ethyl]oxycarbonyl-1,2,3,4-tetrahydroquinoxalin-2-one
https://huagongshe.com/reaction/1378773
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,3-Dimethyl-1,2,3,4-tetrahydroquinoxalin-2-one | HCID 595203 | — |
| Reactant | 4-Chlorocarbonyl-3,3-dimethyl-1,2,3,4-tetrahydroquinoxalin-2-one | HCID 22912818 | — |
| Reactant | 6-Fluoro-3,3-dimethyl-3,4-dihydro-1H-quinoxalin-2-one | HCID 22912892 | — |
| Reactant | Lithium propan-2-olate | HCID 23673350 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 3,3-Dimethyl-4-[(1-methyl)ethyl]oxycarbonyl-1,2,3,4-tetrahydroquinoxalin-2-one | HCID 22912845 | — |
Reaction Steps
To 2.28 g of 4-chlorocarbonyl-3,3-dimethyl-1,2,3,4-tetrahydroquinoxalin-2-one (prepared by the method of Example 32 but using 3,3-dimethyl-1,2,3,4-tetrahydroquinoxalin-2-one rather than 6-fluoro-3,3-dimethyl-1,2,3,4-tetrahydroquinoxalin-2-one) in 25 ml of 2-propanol (the starting material is not all in solution) are added 0.694 g of lithium isopropoxide. After about 1.5 hr the reaction mixture became homogeneous and then again heterogeneous as the product precipitated out. After a total of 2 hr the solvent is removed under reduced pressure and the residue is partitioned between dichloromethane and saline. The organic layers are dried over sodium sulfate and the filtrate is concentrated. Ether is added and the resulting solid is collected to give the title compound, NMR (CDCl3) 1.28, 1.63, 5.01, 6.80, 6.98-7.11, 7.27, 7.96 δ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05668282 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-1bfd486817994e32ad19f42d8d0e179f |
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| Source note | uspto-grants-1997_09 |
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