HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672280Generated: October 30, 2026
Water → 3,3-Dimethyl-1,2,3,4-tetrahydroquinoxalin-2-one
https://huagongshe.com/reaction/1672280
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Propanoic acid, 2-bromo-2-methyl-, ethyl ester | HCID 11745 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3,3-Dimethyl-1,2,3,4-tetrahydroquinoxalin-2-one | HCID 595203 | 57.5% |
Reaction Steps
To a solution of 1,2-phenylenediamine (16.96 g) in N,N-dimethylformamide (80 ml) were added successively N,N-diisopropylethylamine (36.4 mL) and ethyl α-bromoisobutyrate (39.8 g), and the mixture was heated at 110° C. for 3 days. After cooling, to the reaction mixture was added cold water and the mixture was extracted with ethyl acetate. The aqueous layer was extracted with ethyl acetate, and the combined organic layer was washed successively with an aqueous 10% HCl solution, water, an aqueous saturated sodium hydrogencarbonate solution and brine, dried over sodium sulfate and concentrated in vacuo. The resultant residue was recrystallized from dichloromethane-n-hexane to give 3,3-dimethyl-3,4-dihydroquinoxalin-2(1H)-one (15.90 g) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998956B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-a0d388a091714027900149043d72b0d6 |
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| Source note | uspto-grants-2011_08 |
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