HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927292Generated: November 2, 2026
Water → 1-(3-Carboxybenzyl)quinazoline-2,4(1H,3H)-dione
https://huagongshe.com/reaction/927292
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 68388893 | HCID 68388893 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(3-Carboxybenzyl)quinazoline-2,4(1H,3H)-dione | HCID 68388782 | 78% |
Reaction Steps
1-(3-methoxycarbonylbenzyl)quinazoline-2,4(1H,3H)-dione (1.6 g, 5.2 mmol), NaOH (0.31 g, 7.7 mmol), water (40 mL) and methanol (40 mL) were added into a 250 mL three-mouth flask. The mixture was refluxed and reacted for 3 hours. The methanol was removed via evaporation under reduced pressure after the reaction was finished. The mixture was adjusted to pH=2-3 by 3N HCl, forming many precipitates. The mixture was filtered and the solid was washed by water and methonal. The solids were dried to give the title compound as white solid (1.2 g, 78% yield). 1H NMR (300 M, DMSO-d6): 13.09 (brs, 1H), 11.77 (s, 1H), 8.01 (dd, J=7.7 and 1.4 Hz, 1H), 7.84-7.80 (m, 2H), 7.66-7.61 (m, 1H), 7.53 (d, J=7.8 Hz, 1H), 7.44 (t, J=7.7 Hz, 1H), 7.27-7.21 (m, 2H), 5.36 (s, 2H). MS: m/z 297.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290460B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-b5c8d0382a1e48858b625b1618edacff |
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| Source note | uspto-grants-2016_03 |
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