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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 853541생성일: 2026년 10월 24일

Water → N-Methyl-4-benzyloxy-2-methylaniline

https://huagongshe.com/ko/reaction/853541

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1H-Benzotriazole-1-methanolHCID 224169—
반응물Sodium borohydrideHCID 4311764—
반응물4-(Benzyloxy)-2-methylanilineHCID 16773053—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-Methyl-4-benzyloxy-2-methylanilineHCID 2293649862.5%

반응 단계

After dissolving 4-benzyloxy-2-methylaniline (6.55 g, 30.72 mmol) in N,N-dimethylformamide (10 ml) and methanol (60 ml), 1H-benzotriazole-1-methanol (4.58 g, 30.72 mmol) was added and the mixture was stirred for 30 minutes at room temperature. N,N-Dimethylformamide (20 ml) was added for complete dissolution of the precipitated crystals, sodium borohydride (2.32 g, 61.44 mmol) was added in small portions at a time at room temperature (internal temperature increase), and the mixture was stirred for 30 minutes. Water was added to the reaction solution, extraction was performed ethyl acetate, the extract was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was adsorbed onto silica gel and purified by silica gel column chromatography (hexane-ethyl acetate) to obtain the title compound (4.364 g, 19.20 mmol, 62.49%) as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07253286B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-a498f4e50f3c4177aa2892464d055671
출처 메모uspto-grants-2007_08