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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6339생성일: 2026년 10월 24일

Acetic Anhydride → 4,6-Bis(1,1-dimethylethyl)-2-[[2-(3-pyridinyl)]ethenyl]-5-pyrimidinol

https://huagongshe.com/ko/reaction/6339

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Sodium AcetateHCID 517045—
반응물4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)methoxy]-alpha-(3-pyridinyl)-2-pyrimidine-ethanolHCID 19007146—
용매TolueneHCID 1140—
생성물4,6-Bis(1,1-dimethylethyl)-2-[[2-(3-pyridinyl)]ethenyl]-5-pyrimidinolHCID 5456663249.8%

반응 조건

온도190 °C

반응 단계

A mixture of 4,6-bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)methoxy]-α-(3 -pyridinyl)-2-pyrimidineethanol (350 mg), sodium acetate (10 g) and acetic anhydride (7 mL) in toluene (100 mL) is heated at reflux for 8 hours. The reaction mixture is cooled and the solvent is evaporated. Dichlorobenzene (30 mL) is added and the reaction mixture is heated at 190° C. for 30 minutes. The reaction mixture is cooled and partitioned between ethyl acetate and water. The aqueous layer is adjusted to pH 4 with 1N HCl. The organic layer is collected and evaporated. Purification of the residue by flash chromatography (silica, 1:1 ethyl acetate/hexane) followed by recrystallization from hexane gives pure 4,6-bis(1,1-dimethylethyl)-2-[[2-(3-pyridinyl)]ethenyl]-5-pyrimidinol (130 mg, 40%); mp 150°-151° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248682
출처 데이터셋uspto-grants-1993_09
ORD IDord-52a1540eb16c4bf9bce3f0fea0589617
출처 메모uspto-grants-1993_09