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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2366498생성일: 2026년 10월 25일

Pyridine → 3-Acetoxy-2-cyclohexen-1-one

https://huagongshe.com/reaction/2366498

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Acetyl chlorideHCID 6367—
반응물1,3-CyclohexanedioneHCID 10434—
용매ChloroformHCID 6212—
생성물3-Acetoxy-2-cyclohexen-1-oneHCID 275544374.2%

반응 단계

According to Scheme 4 Step 1: Acetyl chloride (19.6 mmol, 1.39 mL) was added to a solution of cyclohexane-1,3-dione (17.8 mmol, 2.00 g) and pyridine (17.8 mmol, 1.28 mL) in CHCl3 (60 mL) and the reaction mixture was stirred at room temperature for 2 hours. The reaction was quenched with the addition of water and the organic phase was washed with a solution of HCl (0.1 M, 30 mL), a saturated solution of NaHCO3 (30 mL) and water (30 mL). The organic phase was dried over Na2SO4 and concentrated to yield 3-oxocyclohex-1-enyl acetate (13.2 mmol, 2.04 g, 74%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08697744B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-02407e83c87e41628812d8e79f688099
출처 메모uspto-grants-2014_04