HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770139Generated: October 29, 2026
Hydrogen Peroxide → HCID 178440202, compound
https://huagongshe.com/reaction/1770139
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | 3-Amino-5-nitrobenzonitrile | HCID 11228974 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178440202 | HCID 178440202 | 54% |
Reaction Steps
To a suspension of 48.94 g (0.3 mol) of 3-nitro-5-amino-benzonitrile in 500 ml of CH2Cl2 was added 63 ml of Et3N, 3 g DMAP and lastly, dropwise, 45.5 g (0.45 mol) of butyryl chloride. A mild exothermic reaction ensued. The mixture was allowed to stir for 2 days (monitor TLC with 50% EtOAc/hexanes). The solution was washed with 1N HCl (2×100 ml), water (1×100 ml) sat. NaHCO3 (2×100 ml), brine (1×100 ml) and dried over MgSO4. The suspension was filtered and concentrated in vacuo. The residue was suspended in a mixture of 600 ml of MeOH and 200 ml of water in a three neck round bottom flask. To this was added gradually 140 ml (0.7 m) of 5N NaOH solution followed by the dropwise addition of 80 ml of 30% H2O2 (0.7 mol) solution (beware of exothermic reaction!). The mixture was refluxed over night, cooled to room temperature and filtered. The filtrate was acidified with 1N HCl cooled to 5° C. and filtered. The quinazolinone may be recrystalized form hot MeOH to give 38 g of pale brown fine crystals. 54% yield. 1H-NMR-CDCl3 :1.10 (t, 3H, J=7.8 Hz), 1.93 (m, 2H), 2.79 (t, 2H, J=7.3 Hz), 7.81 (d, 1H, J=8.9 Hz), 8.55 (dd, 1H, J=2.4, 8.8 Hz), 9.14 (d, 1H, J=2.4 Hz), 10.72 (bs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05385894 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-90adf15152134bf1ae305defaf55db74 |
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| Source note | uspto-grants-1995_01 |
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