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HRID 339361Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/339361

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium HydroxideHCID 14798—
Edukt(R)-N-(1-hydroxy-4-methylpentan-2-yl)-3,4-dimethylbenzamideHCID 39352414—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-((1R)-1-(Methoxymethyl)-3-methylbutyl)-3,4-dimethylbenzamideHCID 5752796473,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895050B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-f79309d3f0de4500876070ea3271a2b9
Quellennotizuspto-grants-2014_11