돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1976152생성일: 2026년 10월 25일

1,4-Dioxa-8-azaspiro(4.5)decane → 1-(5-Cyano-2-methoxyphenyl)-4-piperidone ethylene ketal

https://huagongshe.com/reaction/1976152

반응식

참여 물질

역할이름HCID투입량
반응물1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
반응물3-Bromo-4-methoxybenzonitrileHCID 736049—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
용매TolueneHCID 1140—
생성물1-(5-Cyano-2-methoxyphenyl)-4-piperidone ethylene ketalHCID 5720032738.2%

반응 조건

온도100 °C

반응 단계

1,4-Dioxa-8-azaspiro[4.5]decane (1.47 g, 10.28 mmol), sodium bis(trimethylsilyl)amide (1 N in THF, 12 ml), and PdCl2(p(o-tolyl)3)2 [2 mol % catalyst prepared from bis(acetonitrile) Pd(II) chloride(53 mg, 0.206 mmol) and tri(o-tolyl)phosphine (125 mg, 0.52 mmol)] were added to a solution of 3-bromo-4-methoxybenzonitrile (1.82 g, 8.58 mmol) in toluene (40 ml). The reaction was stirred for 5 hours at 100° C. The reaction was concentrated in vacuo, diluted with water, and extracted with methylene chloride. The organic extract was concentrated in vacuo, and the residue purified by chromatography on silica gel using hexane/ethyl acetate (80/20) as the eluent to give 1-(5-cyano-2-methoxyphenyl)-4-piperidone ethylene ketal (900 mg, 38%). This ketal was dissolved in dioxane (15 ml) and HCl (6 N, 2.2 ml) and stirred at 100° C. for 2 h. The solution was cooled, quenched with saturated aqueous NaHCO3. The mixture was extracted with methylene chloride, concentrated in vacuo, and purified by chromatography on silica gel using hexane/ethyl acetate (80/20) as the eluent to give 1-(5-cyano-2-methoxyphenyl)-4-piperidone (125 mg, 19%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06225324B1
출처 데이터셋uspto-grants-2001_05
ORD IDord-38f4bfe42b794dafb365af318b2d0579
출처 메모uspto-grants-2001_05