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HRID 339361作成日:2026年10月26日

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

https://huagongshe.com/reaction/339361

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium HydroxideHCID 14798—
反応物(R)-N-(1-hydroxy-4-methylpentan-2-yl)-3,4-dimethylbenzamideHCID 39352414—
溶媒DimethylformamideHCID 6228—
生成物N-((1R)-1-(Methoxymethyl)-3-methylbutyl)-3,4-dimethylbenzamideHCID 5752796473.1%

反応条件

温度0 °C

反応手順

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)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895050B2
出典データセットuspto-grants-2014_11
ORD IDord-f79309d3f0de4500876070ea3271a2b9
出典メモuspto-grants-2014_11