HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10242Generated: October 27, 2026
Diethyl 2-(p-tolyl)malonate → HCID 178418910, compound
https://huagongshe.com/reaction/10242
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl 2-(p-tolyl)malonate | HCID 570878 | — |
| Reactant | Methanimidamide, hydrochloride (1:1) | HCID 10313058 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178418910 | HCID 178418910 | 97.6% |
Reaction Steps
At 0° C. a solution of diethyl 2-(p-tolyl)-malonate (14.2 g) in methanol (50 ml) was slowly added to a solution of sodium methylate (9.4 g) in methanol (300 ml). Upon completion of the addition the reaction mixture was allowed to warm up and formamidine hydrochloride (5.4 g) was added. The mixture was stirred at r.t. for 16 h. The solvent was removed under reduced pressure and the remaining residue was treated with 2 N hydrochloric acid (150 ml). The suspension was stirred for 0.5 h. At 0–5° C., the pH was carefully adjusted to 4 using 10 N sodium hydroxide solution. The precipitate was collected, washed with cold water, isopropanol, and diethyl ether and dried under high vacuum at 65° C. to give 4,6-dihydroxy-5-(p-tolyl)-pyrimidine (11.2 g) (or a tautomer) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07094781B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-5f2fb7b342c44f879faf621a08f0c6ed |
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| Source note | uspto-grants-2006_08 |
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