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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75510생성일: 2026년 10월 25일

Acetone → 1-(Pyridin-3-yl)butane-1,3-dione

https://huagongshe.com/reaction/75510

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물Ethyl NicotinateHCID 69188—
용매TetrahydrofuranHCID 8028—
생성물1-(Pyridin-3-yl)butane-1,3-dioneHCID 300160—

반응 단계

A cooled (0° C.) solution of ethyl nicotinate (3.00 g, 2.71 ml, 19.65 mmol) in THF (10 ml) was treated with sodium hydride (60%, 1.572 g, 39.3 mmol) followed by the dropwise addition of a solution of acetone (2.282 g, 39.3 mmol, 2.89 ml) in THF (10 ml). The mixture was heated at reflux for 3 hours and then allowed to cool to RT. The mixture was acidified to ˜pH5 with 2M HCl and partitioned between EtOAc and water. The organic phase was separated and washed with water, brine, dried (MgSO4) filtered and the solvent was removed in vacuo. Purification by chromatography on silica eluting with iso-hexane/EtOAc afforded the titled compound; 1H NMR (CDCl3, 400 MHz) δ 15.97 (1H, s), 9.10 (1H, s), 8.78 (1H, d), 8.22 (1H, d), 7.49 (1H, t), 6.21 (1H, s), 2.25 (3H, s). LCMS Rt=1.13 mins; [M+H]+ 164.21 Method LowpH_v002.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835444B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ebf9e313d559476a8fb1a6ce9712deae
출처 메모uspto-grants-2014_09