HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267153Generated: November 1, 2026
4-Bromophenacyl bromide → HCID 18545776, compound
https://huagongshe.com/reaction/1267153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | 3-Oxo-1,2,3,4-tetrahydroquinoxaline-6-carbonitrile | HCID 10797301 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18545776 | HCID 18545776 | 37.8% |
Reaction Steps
To a solution of 7-cyano-3,4-dihydroquinoxalin-2(1H)-one (4 mg, 20 mmol) in THF (100 mL) was added K2CO3 (152 mg, 1.1 mmoL), 18-crown-6 (230 mg), and 2,4′-dibromoacetophenone (5.54 g, 20 mmol), and the resulting mixture was stirred for 16 hours. The mixture was diluted with EtOAc and filtered. The residue was washed with EtOAc and water, and dried by air to give the product (2.8 g, 37.8%). The filtrate was washed with brine (50 mL×4), dried over MgSO4, and concentrated to give a crude material, which was recrystallized in EtOAc (20 mL) to give the product (2 g, 27%) as a white solid. 1H NMR (DMSO-d6) δ 8.02 (d, J=8.4 Hz, 2H), 7.83 (d, J=8.4 Hz, 2H), 7.35 (d, J=1.4 Hz, 1H), 7.26 (dd, J=8.1 Hz, J=1.4 Hz, 1H), 7.10 (s, 1H), 6.81 (d, J=8.4 Hz, 1H), 5.50 (s, 2H), 4.05 (d, J=1.1 Hz, 2H); MS(CI) m/z 370/372 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06552042B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-6685399e63744e66b03f68b4899f5fbd |
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| Source note | uspto-grants-2003_04 |
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