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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272321생성일: 2026년 10월 25일

Dimethyl Sulfate → N-(4-methoxy-2,3,6-trimethylphenyl)formamide

https://huagongshe.com/reaction/272321

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfateHCID 6497—
반응물Potassium HydroxideHCID 14797—
반응물N-(4-hydroxy-2,3,6-trimethylphenyl)formamideHCID 21961295—
용매MethanolHCID 887—
생성물N-(4-methoxy-2,3,6-trimethylphenyl)formamideHCID 21961345—

반응 단계

N-(4-Hydroxy-2,3,6-trimethylphenyl)formamide (30.0 g, 167 mmol) was dissolved into a mixed solvent of a 4 N aqueous solution of potassium hydroxide (100 ml) and methanol (300 ml) and dimethyl sulfate (42.0 g, 334 mmol) was added to the resulting solution at room temperature. The resulting mixture was refluxed with heating for 14 hours. After the reaction solution was cooled down, the crystals precipitated were collected by filtration to obtain N-(4-methoxy-2,3,6-trimethylphenyl)formamide as a crude product. To a suspension of this compound in methanol (200 ml) was added concentrated hydrochloric acid (50 ml) and the resulting mixture was refluxed with heating for 3 hours. The reaction mixture was cooled down and neutralized with an 8 N aqueous solution of sodium hydroxide. The product was extracted twice with ethyl acetate. The combined extracts were washed with a 10% aqueous solution of sodium hydrosulfite, dried on magnesium sulfate, and then concentrated under reduced pressure. The residue was crystallized from isopropyl ether to obtain 21.0 g (yield 76%) of the title compound. Melting point: 70-72° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456162B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-24e5812ba931462eb63b82dfa5fc8e85
출처 메모uspto-grants-2008_11