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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21615생성일: 2026년 10월 25일

Methyl iodide → 3,5-DI-Tert-butyl-4-methoxybenzaldehyde

https://huagongshe.com/reaction/21615

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium HydroxideHCID 14798—
반응물Methane, dichloromethoxy-HCID 21004—
반응물Tin tetrachlorideHCID 24287—
반응물2,6-Di-tert-butylphenolHCID 31405—
촉매Benzyl triethylammonium chlorideHCID 66133—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물3,5-DI-Tert-butyl-4-methoxybenzaldehydeHCID 1291093947.7%

반응 단계

A mixture containing 2 g (9.7 mmol) 2,6-di-tert-butyl phenol, 0.4 g NaOH dissolved in 4 ml water, 13.7 g (60.1 mmol) benzyl triethyl ammonium chloride and 12 g (84.5 mmol) methyl iodide was heated at 45° for 18 h. After purification 0.67 g 2,6-di-tert-butyl anisol was obtained. This compound (1.46 g, 6.63 mmol) was formylated by reaction at 0° C. with dichloromethyl methyl ether (1.15 g, 10 mmol) in presence of tin tetrachloride (3.1 g, 11.9 mmol) in 20 ml CH2Cl2. After hydrolysis and extraction into ether, 1.15 g of 3,5-di-tert-butyl-4-methoxybenzaldehyde were obtained (MS: m/e=248: M+; 233=M+ --CH3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424303
출처 데이터셋uspto-grants-1995_06
ORD IDord-10bd30426ab0424eb72c822219e8e9e9
출처 메모uspto-grants-1995_06