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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1168091생성일: 2026년 10월 24일

Methyl iodide → 4-(2,6-Dichloro-4-methoxymethyl-phenoxy)-anisole

https://huagongshe.com/ko/reaction/1168091

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물3,5-Dichloro-4-(4-methoxyphenoxy)benzyl AlcoholHCID 22285654—
반응물HCID 178418361HCID 178418361—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-(2,6-Dichloro-4-methoxymethyl-phenoxy)-anisoleHCID 2228565997.7%

반응 단계

To a solution of the title compound of Step A (400 mg, 1.34 mmol) in dry dimethylformamide (13 mL) at 0° C. under nitrogen was added NaH (60% dispersion in mineral oil, 134 mg, 3.3 mmol). After stirring for 30 minutes at 0° C. until hydrogen evolution ceased, methyl iodide (949 mg, 6.61 mmol) was added. The reaction mixture was warmed to room temperature and stirred for about 19 hours. The solution was poured into water (100 ml) and extracted with ethyl acetate (3×100 ml). The combined extracts were washed with 1M HCl (3×100 ml), brine (100 ml), dried, filtered, and concentrated. The crude product was purified by preparative TLC (30% hexane in dichloromethane) to afford the title compound (410 mg). NMR (400 MHz, CDCl3) δ7.36 (s, 2H), 6.75-6.83 (m, 4H), 4.40 (s, 2H), 3.75 (s, 3H), 3.43 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06620830B2
출처 데이터셋uspto-grants-2003_09
ORD IDord-567f5fcc4362481db6593d829cf33380
출처 메모uspto-grants-2003_09