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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 431415생성일: 2026년 10월 26일

Pyridine → alpha-[Acetoxy(5-norbornen-2-yl)methyl]-gamma-butyrolactone

https://huagongshe.com/reaction/431415

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Acetic AnhydrideHCID 7918—
반응물3-[(Bicyclo[2.2.1]hept-5-en-2-yl)(hydroxy)methyl]oxolan-2-oneHCID 18345689—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
생성물alpha-[Acetoxy(5-norbornen-2-yl)methyl]-gamma-butyrolactoneHCID 1876107298%

반응 단계

To 127 g of pyridine were added 208 g of α-[hydroxy(5-norbornen-2-yl)methyl]-γ-butyrolactone (Monomer 1), 123 g of acetic anhydride and 6 g of 4-dimethylaminopyridine. Reaction was effected at 25° C. for 10 hours. Water, 30 g, was added to the reaction mixture to stop reaction, followed by hexane extraction. The organic layer was washed with water, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuum. Purification by silica gel column chromatography yielded 245 g (yield 98%) of α-[acetoxy(5-norbornen-2-yl)methyl]-γ-butyrolactone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06660448B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-77154b4f71174c1f8296e946b2bfb9b2
출처 메모uspto-grants-2003_12