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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 917384생성일: 2026년 10월 26일

Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl ester → HCID 12194769, 화합물

https://huagongshe.com/reaction/917384

반응식

참여 물질

역할이름HCID투입량
반응물Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl esterHCID 97734—
반응물Sodium AcetateHCID 517045—
반응물2-Phenylethanimidamide hydrochlorideHCID 12415514—
용매DimethylformamideHCID 6228—
생성물HCID 12194769HCID 1219476989%

반응 조건

온도100 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07273878B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-22aa77e03b3042448a53c53288fa8fe5
출처 메모uspto-grants-2007_09