돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 746264생성일: 2026년 10월 23일

4-Hydroxy-2,2,6,6-tetramethylpiperidine → 2,2,6,6-Tetramethylpiperidin-4-yl 2,5-dimethylfuran-3-carboxylate

https://huagongshe.com/ko/reaction/746264

반응식

참여 물질

역할이름HCID투입량
반응물4-Hydroxy-2,2,6,6-tetramethylpiperidineHCID 75471—
반응물3-Furancarboxylic acid, 2,5-dimethyl-, methyl esterHCID 80248—
촉매TetrabutoxytitaniumHCID 521701—
용매MethanolHCID 887—
생성물2,2,6,6-Tetramethylpiperidin-4-yl 2,5-dimethylfuran-3-carboxylateHCID 13765634—

반응 단계

154 g (1 mole) of methyl 2,5-dimethylfuran-3-carboxylate and 157 g (1 mole) of 4-hydroxy-2,2,6,6-tetramethylpiperidine were heated together with 10 g of tetrabutyl orthotitanate for 10 hours at about 190° C., the methanol formed being distilled off. When the reaction is complete, the mixture is cooled and the reaction mass is dissolved in ethyl acetate. The solution is extracted by shaking, first with 10% strength sodium carbonate solution and then with water, after which it is dried and evaporated down, and the residue is distilled under reduced pressure. The desired product distils at 142° C./2 mm as a virtually colorless oil which soon solidifies to a solid of melting point 59°-61° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04603205
출처 데이터셋uspto-grants-1986_07
ORD IDord-66b19aa7576741619657092ed9d7f36e
출처 메모uspto-grants-1986_07