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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488064생성일: 2026년 10월 25일

Hydrochloric Acid → 2-(1,3-Dioxolan-2-yl)ethyl 2-(4,6-dimethoxypyrimidin-2-yl)oxybenzoate

https://huagongshe.com/reaction/488064

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물2-(2-Bromoethyl)-1,3-dioxolaneHCID 87776—
반응물2-((4,6-Dimethoxypyrimidin-2-yl)oxy)benzoic acidHCID 184185—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
생성물2-(1,3-Dioxolan-2-yl)ethyl 2-(4,6-dimethoxypyrimidin-2-yl)oxybenzoateHCID 1527823763.8%

반응 단계

10 Milliliters of N,N-dimethylformamide in which 0.22 g of 60% sodium hydride in oil has been suspended was mixed with 5 ml of N,N-dimethylformamide solution of 1.38 g of 2-(4,6-dimethoxypyrimidin-2-yl)oxy benzoic acid. After stirring the mixture at room temperature for 30 minutes, 10 ml of N,N-dimethylformamide solution of 1.81 g of 2-(2-bromoethyl)-1,3-dioxolane was added thereto. The resulting solution was stirred at 100° to 110° C. for 2 hours. The reaction solution was allowed to cool, poured into diluted hydrochloric acid, and extracted with ethyl acetate. The organic layer separated from the aqueous layer was washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue obtained was subjected to silica gel column chromatography (mfd. by Merck & Co., Inc., solvent: chloroform) to obtain 1.20 g of 2-(1,3-dioxolan-2-yl)ethyl 2-(4,6-dimethoxypyrimidin-2-yl)oxybenzoate [present compound (V-2)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05298632
출처 데이터셋uspto-grants-1994_03
ORD IDord-57289cd2ff5e490b8cb79b1e767d633f
출처 메모uspto-grants-1994_03