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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 383257생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/383257

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ethoxideHCID 2723922—
반응물Mucobromic AcidHCID 3033972—
반응물SodiumHCID 5360545—
반응물Propionimidamide hydrochlorideHCID 12301253—
용매EthanolHCID 702—
생성물5-Bromo-2-ethylpyrimidine-4-carboxylic acidHCID 6697770237%

반응 조건

온도55 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367663B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-d3a42bce36734cdfa320fdae2d93aa99
출처 메모uspto-grants-2013_02