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HRID 917384作成日:2026年10月26日
Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl ester → Ethyl 2-benzyl-4-methylpyrimidine-5-carboxylate
https://huagongshe.com/reaction/917384
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl ester | HCID 97734 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | 2-Phenylethanimidamide hydrochloride | HCID 12415514 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Ethyl 2-benzyl-4-methylpyrimidine-5-carboxylate | HCID 12194769 | 89% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07273878B2 |
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| 出典データセット | uspto-grants-2007_09 |
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| ORD ID | ord-22aa77e03b3042448a53c53288fa8fe5 |
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| 出典メモ | uspto-grants-2007_09 |
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