HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682106Generated: October 31, 2026
2,3-Dihydro-1,4-benzodioxin-6-carbaldehyde → HCID 14795475, compound
https://huagongshe.com/reaction/1682106
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dihydro-1,4-benzodioxin-6-carbaldehyde | HCID 248127 | — |
| Reactant | 5,6-Diamino-1,3-dipropyl-2,4(1H,3H)-pyrimidinedione | HCID 5098605 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14795475 | HCID 14795475 | 92.2% |
Reaction Steps
2.18 g (0.013 mol) of 1,4-benzodioxan-6-aldehyde, 80 ml of ethanol and 2.4 ml of glacial acetic acid are mixed together and 2.8 g (0.012 mol) of 5,6-diamino-1,3-dipropyluracil are added thereto. The clear solution is refluxed for 21/4 hours and then cooled to 60° C. At this temperature, 2.1 ml (0.013 mol) of diethylazodicarboxylate are added dropwise and the viscous suspension produced is mixed with 80 ml of ethanol and refluxed for 2 hours. After a further 20 hours at ambient temperature the mixture is cooled to 5° C., the solid matter is filtered under suction and washed with ethanol and ether. 4.1 g of the title compound are obtained in the form of a grey solid (=92% of theory), melting point 280°-282° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05175291 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-18439dd3695d4890935de1ba53ef288e |
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| Source note | uspto-grants-1992_12 |
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