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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1644068생성일: 2026년 10월 26일

Chloromethyl Methyl Ether → (R)-N-(1-(methoxymethoxy)-4-methylpentan-2-yl)-3,4-dimethylbenzamide

https://huagongshe.com/reaction/1644068

반응식

참여 물질

역할이름HCID투입량
반응물Chloromethyl Methyl EtherHCID 7864—
반응물Sodium HydroxideHCID 14798—
반응물(R)-N-(1-hydroxy-4-methylpentan-2-yl)-3,4-dimethylbenzamideHCID 39352414—
용매DimethylformamideHCID 6228—
생성물(R)-N-(1-(methoxymethoxy)-4-methylpentan-2-yl)-3,4-dimethylbenzamideHCID 5752795253%

반응 조건

온도0 °C

반응 단계

To a solution of (R)—N-(1-hydroxy-4-methylpentan-2-yl)-3,4-dimethylbenzamide (Example 71a) (0.24 mmol) dissolved in dry DMF (2 mL) was added at 0° C. powdered NaOH (0.36 mmol, 14.5 mg, 1.5 eq) and the mixture was stirred for 1 hr at 0° C. Then chloro-methoxy-methane (19.3 μl, 1 eq) was added and the reaction stirred at 0° C. for 1 hour. The reaction was quenched with water (30 mL) and the mixture was extracted with dichloromethane. The organic phase was dried over MgSO4 and evaporated. The crude product was purified by preparative TLC (20% ethyl acetate/hexanes) to give 37.7 mg of (R)—N-(1-(methoxymethoxy)-4-methylpentan-2-yl)-3,4-dimethylbenzamide (53%). 1H NMR (500 MHz, CDCl3): δ 0.98-1.00 (t, 6H), 1.49-1.53 (m, 1H), 1.58-1.64 (m, 1H), 1.69-1.73 (m, 2H), 2.32-2.33 (d, 6H), 3.38-3.39 (t, 3H), 3.64-3.72 (ddd, 2H), 4.41-4.44 (m, 1H), 4.65-4.69 (dd, 2H), 6.37-6.39 (d, 1H), 7.19-7.21 (d, 1H), 7.50-7.52 (dd, 1H), 7.60 (sb, 1H). MS (M+H, 294.3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08124121B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-f63d130e191247cb821713b16b4cff8d
출처 메모uspto-grants-2012_02