참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl ester | HCID 97734 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 반응물 | 2-Phenylethanimidamide hydrochloride | HCID 12415514 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | HCID 12194769 | HCID 12194769 | 89% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07273878B2 |
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| 출처 데이터셋 | uspto-grants-2007_09 |
|---|
| ORD ID | ord-22aa77e03b3042448a53c53288fa8fe5 |
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| 출처 메모 | uspto-grants-2007_09 |
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