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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899956Generated: November 1, 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/1899956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-Dimethyl-1,2,3,4-tetrahydroquinoxalin-2-oneHCID 595203—
Reactant4-Chlorocarbonyl-3,3-dimethyl-1,2,3,4-tetrahydroquinoxalin-2-oneHCID 22912818—
Reactant6-Fluoro-3,3-dimethyl-3,4-dihydro-1H-quinoxalin-2-oneHCID 22912892—
ReactantLithium propan-2-olateHCID 23673350—
SolventIsopropanolHCID 3776—
Product3,3-Dimethyl-4-[(1-methyl)ethyl]oxycarbonyl-1,2,3,4-tetrahydroquinoxalin-2-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574038
Source datasetuspto-grants-1996_11
ORD IDord-cad7337061f2406498f36099b06f3a1d
Source noteuspto-grants-1996_11