HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358967Generated: November 1, 2026
Acetic Acid → 6-Bromo-3,4-dihydro-4-methyl-2(1H)-quinoxalinone
https://huagongshe.com/reaction/2358967
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 6-Bromo-1,2,3,4-tetrahydroquinoxalin-2-one | HCID 66911307 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Bromo-3,4-dihydro-4-methyl-2(1H)-quinoxalinone | HCID 22667740 | 94% |
Reaction Steps
To a solution of 6-bromo-3,4-dihydroquinoxalin-2(1H)-one (370 mg, 1.63 mmol) in 10 ml methanol was added a solution of 37% formaldehyde in water (59 mg, 1.95 mmol) and acetic acid (196 mg, 3.26 mmol). The mixture was stirred at room temperature for 2 h, then refluxed for 1 h. After addition of NaBH3CN (307 mg, 4.89 mmol) stirring was continued for 2.5 h at room temperature. Then methanol was removed under vacuum. To the remaining mixture water was added. Then the solution was basified to pH 8-9 with an aqueous solution of sodium hydrogen carbonate and extracted several times with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4 and evaporated, affording 6-bromo-4-methyl-3,4-dihydroquinoxalin-2(1H)-one (369 mg, 1.53 mmol, 94%) as off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08685960B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-f9175441841f47ea800a8ab9c4b3cc3a |
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| Source note | uspto-grants-2014_04 |
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