HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dimethoxybenzene → 5-Methoxy-2-thioxodihydropyrimidine-4,6(1H,5H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dimethoxybenzene | HCID 9025 | — |
| Reactant | 2,7-Dimethoxynaphthalene | HCID 77021 | — |
| Reactant | Thiobarbituric acid | HCID 2723628 | — |
| Product | 5-Methoxy-2-thioxodihydropyrimidine-4,6(1H,5H)-dione | HCID 21912476 | — |
Reaction Steps
The Birch reduction products of 1,3-dimethoxybenzene and of 2,7-dimethoxynaphthalene each react with thiobarbituric acid to form the conjugated methoxy-thiobarbituric acid dyes as shown in FIG. 13. For this reaction, no solvent is used. The reactants were melted at 145° C. for 15 min. Methanol condensing at the walls of the flask showed successful reaction. Purification was carried out by simple filtration over a short column of SiO2 with CH2Cl2. Yields were typically around 60%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06402994B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-cd567366b2dd4a79aff2c95ae57aee00 |
| Source note | uspto-grants-2002_06 |