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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

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 numberUS05668282
Source datasetuspto-grants-1997_09
ORD IDord-1bfd486817994e32ad19f42d8d0e179f
Source noteuspto-grants-1997_09