戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1255800作成日:2026年10月27日

Sodium ethoxide → 5-Bromo-2-ethylpyrimidine-4-carboxylic acid

https://huagongshe.com/reaction/1255800

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ethoxideHCID 2723922—
反応物Mucobromic AcidHCID 3033972—
反応物SodiumHCID 5360545—
反応物Propionimidamide hydrochlorideHCID 12301253—
溶媒EthanolHCID 702—
生成物5-Bromo-2-ethylpyrimidine-4-carboxylic acidHCID 6697770237%

反応条件

温度55 °C

反応手順

Sodium (356 mg, 15.5 mmol) was carefully added to ethanol (5.9 mL) to prepare sodium ethoxide solution in ethanol. The above freshly prepared ethanol solution (3.5 mL) was added to a stirred suspension of propionimidamide hydrochloride (1.05 g, 9.69 mmol). The mixture was warmed to 55° C., then the heating bath was removed and a solution of mucobromic acid (1 g, 3.87 mmol) in ethanol was added dropwise at a rate which maintained a constant temperature, followed by a further sodium ethoxide solution (2 mL). After cooling, the mixture was filtered and evaporated to a residue which was shaken vigorously with hydrochloric acid (2 M×2.4 mL). The brown precipitate was filtered off and washed with cold water, then freeze-dried to give 5-Bromo-2-ethylpyrimidine-4-carboxylic acid (330 mg, 37%) as a yellow solid. LCMS: 231 [M+1]+, 1H NMR (400 MHz, DMSO-d6): δ 1.25 (t, J=7.6 Hz, 3H), 2.88 (q, J=7.6 Hz, 2H), 9.05 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08461157B2
出典データセットuspto-grants-2013_06
ORD IDord-50672b3b031641a89651b56c4c1cebcc
出典メモuspto-grants-2013_06