HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917384Generated: October 26, 2026
Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl ester → HCID 12194769, compound
https://huagongshe.com/reaction/917384
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl ester | HCID 97734 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-Phenylethanimidamide hydrochloride | HCID 12415514 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12194769 | HCID 12194769 | 89% |
Reaction Steps
To 100 ml of N,N-dimethylformamide, 17.1 g (100 mmol) of 2-phenylacetoamidine hydrochloric acid salt, synthesized in accordance with a method described in “Tetrahedron”, page 887 (1984), 18.6 g (100 mmol) of ethyl 2-acetyl-3-ethoxyacrylate and 9.0 g (110 mmol) of sodium acetate were suspended, followed by stirring at 100° C. for 3 hours. The reaction liquid was cooled and then poured into ice water, and extracting with diethyl ether. The organic layer was washed with water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentrating under reduced pressure to obtain 22.8 g (yield: 89%) of ethyl 2-benzyl-4-methylpyrimidine-5-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07273878B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-22aa77e03b3042448a53c53288fa8fe5 |
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| Source note | uspto-grants-2007_09 |
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