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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11984생성일: 2026년 10월 24일

Triethylamine → 2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-N-(2'-iodo-6'-methoxyphenyl)acetamide

https://huagongshe.com/ko/reaction/11984

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Chloro-1-methylpyridinium iodideHCID 167069—
반응물2-(1,4-Dioxaspiro[4.5]dec-7-en-8-yl)acetic acidHCID 11287090—
반응물2-Iodo-6-methoxyanilineHCID 11379663—
용매DichloromethaneHCID 6344—
생성물2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-N-(2'-iodo-6'-methoxyphenyl)acetamideHCID 2195169089.6%

반응 단계

A solution of (1,4-dioxaspiro[4.5]dec-7-en-8-yl) acetic acid (567 mg; 2.86 mmol; 1 eq) (7) and 2-iodo-6-methoxyaniline (1 g; 2.86 mmol; 1 eq) in anhydrous dichloromethane (30 mL) is admixed with 2-chloro-1-methylpyridinium iodide (1.46 g; 5.73 mmol; 2 eq) and triethylamine (3.98 mL; 28.65 mmol; 10 eq). The reaction mixture is heated at reflux for 20 hours. After cooling and acidification with 1N HCl solution to pH=5-6, the mixture is extracted with dichloromethane. The organic phases are washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate and evaporated under vacuum. Purification by flash chromatography on silica gel (eluent: heptane/ethyl acetate 4/6) gives 1.10 g of 2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-N-(2′-iodo-6′-methoxy-phenyl)acetamide (16) in the form of a yellow foam (yield: 90%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE041366E1
출처 데이터셋uspto-grants-2010_06
ORD IDord-d73a86df4d0d4a32a23007aeff1a94e4
출처 메모uspto-grants-2010_06