HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098599Generated: October 25, 2026
Diethyl (ethoxymethylene)malonate → HCID 178469768, compound
https://huagongshe.com/reaction/1098599
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Propanimidamide, 2,2-dimethyl-, hydrochloride (1:1) | HCID 2781880 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178469768 | HCID 178469768 | 36% |
Reaction Steps
In ethanol (40 mL) was placed t-butylcarbamidine hydrochloride (3.71 g, 27.2 mmol). This was treated with 21% sodium ethoxide in ethanol (8.80 g, 27.2 mmol) and stirred at RT for 15 min. To this was added the diethyl ethoxymethylenemalonate (5.87 g, 27.2 mmol) and the reaction mixture was stirred overnight at RT. The reaction mixture was refluxed for 1 hour and then cooled to RT. The solution was evaporated, the residue dissolved in water (100 mL) and the pH adjusted to 3-4 (wet litmus) with acetic acid. The mixture formed a precipitate. The solid collected by filtration, washed with water (50 mL) and dried in vacuo to obtain ethyl 2-tert-butyl-4-hydroxypyrimidine-5-carboxylate (2.18 g, 36% yield). 1H NMR (400 MHz, DMSO-d6): δ 12.6 (brs, 1H), 8.44 (s, 1H), 4.20 (q, J=7.2 Hz, 2H), 1.25 (s, 9H), 1.23 (t, J=7.2 Hz, 3H); MS (ESI) m/z: 225.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143293B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-d3a2b9334cb847d9ad63b01db73f2fe6 |
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| Source note | uspto-grants-2012_03 |
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