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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339361생성일: 2026년 10월 25일

Methyl iodide → N-((1R)-1-(Methoxymethyl)-3-methylbutyl)-3,4-dimethylbenzamide

https://huagongshe.com/reaction/339361

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참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium HydroxideHCID 14798—
반응물(R)-N-(1-hydroxy-4-methylpentan-2-yl)-3,4-dimethylbenzamideHCID 39352414—
용매DimethylformamideHCID 6228—
생성물N-((1R)-1-(Methoxymethyl)-3-methylbutyl)-3,4-dimethylbenzamideHCID 5752796473.1%

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온도0 °C

반응 단계

To a solution of (R)—N-(1-hydroxy-4-methylpentan-2-yl)-3,4-dimethylbenzamide (1.59 g, 6.39 mmol) (example 71a) in dry DMF (20 mL) was added powdered NaOH (281 mg, 7 mmol) an the solution was stirred at 0° C. for 2 hrs. Iodomethane (1 eq, 6.39 mmol) was added in DMF (10 ml) drop-wise over period of 1 hr. The temperature was kept at 0° C. and the mixture was stirred for 1 hr. The reaction was quenched by adding 300 ml of water. The aqueous layer was extracted with dichloromethane, dried over MgSO4 and evaporated. The residue was purified by flash chromatography on silica-gel (toluene-ethyl acetate; 5-20% gradient) to give 1.23 g (R)—N-(1-methoxy-4-methylpentan-2-yl)-3,4-dimethylbenzamide (73%). 1H NMR (500 MHz, CDCl3): δ 0.94-0.97 (t, 6H), 1.41-1.47 (M, 1H), 1.54-1.60 (m, 1H), 1.64-1.68 (m, 1H), 2.29 (d, 6H), 3.36 (s, 3H), 3.45-3.50 (m, 2H), 4.34-4.39 (m, 1H), 6.23-6.25 (d, 1H), 7.16-7.17 (d, 1H), 7.47-7.49 (dd, 1H), 7.56 (s, 1H). MS (M+H, 264.3)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895050B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-f79309d3f0de4500876070ea3271a2b9
출처 메모uspto-grants-2014_11