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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736715Generated: October 30, 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/1736715

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 aid 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 numberUS05541324
Source datasetuspto-grants-1996_07
ORD IDord-2eb2b14573524857a621271aecb4c9f7
Source noteuspto-grants-1996_07