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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488065생성일: 2026년 10월 24일

Hydrochloric Acid → Tetrahydrofurfuryl 2-(4,6-dimethoxypyrimidin-2-yl)oxybenzoate

https://huagongshe.com/ko/reaction/488065

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1-MethylimidazoleHCID 1390—
반응물2,4,6-Tris(1-methylethyl)benzenesulfonyl chlorideHCID 81042—
반응물Tetrahydro-2-hydroxyfuranHCID 93002—
반응물2-((4,6-Dimethoxypyrimidin-2-yl)oxy)benzoic acidHCID 184185—
용매ChloroformHCID 6212—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Tetrahydrofurfuryl 2-(4,6-dimethoxypyrimidin-2-yl)oxybenzoateHCID 15278238—

반응 단계

0.55 Gram of 2-(4,6-dimethoxypyrimidin-2-yl)oxybenzoic acid, 0.21 g of tetrahydrofuryl alcohol and 0.85 g of 2,4,6-triisopropylbenzenesulfonyl chloride were dissolved in 5 ml of tetrahydrofuran. Subsequently, 0.45 g of 1-methylimidazole was added to the mixture. After stirring the resulting solution at room temperature for 1 hour in order to carry out the reaction, the reaction solution was poured into diluted hydrochloric acid, and exracted 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 Merch & Co., Inc., solvent: chloroform) to obtain 0.30 g of tetrahydrofurfuryl 2-(4,6-dimethoxypyrimidin-2-yl)oxybenzoate [present compound (III-9)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05298632
출처 데이터셋uspto-grants-1994_03
ORD IDord-c5e8126c74af475bbb87348101a348c0
출처 메모uspto-grants-1994_03