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HRID 1690726Erstellt: 26. Oktober 2026

Methyl iodide → 4-(5-Methoxymethyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-one

https://huagongshe.com/reaction/1690726

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
Edukt4-(5-Hydroxymethyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-oneHCID 57781122—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(5-Methoxymethyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-oneHCID 24802691—

Reaktionsschritte

To a solution of 4-(5-hydroxymethyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-one (0.125 g, 0.495 mmol) (Example 6d) in DMF (2 mL) is added sodium hydride (0.018 g, 0.495 mmol). The reaction mixture is stirred at room temperature for 5 min and then methyl iodide (0.028 mL, 0.495 mmol) is added. The reaction is stirred for 2.5 h at room temperature. It is then washed with water and extracted with ethyl acetate twice. The organic layer is dried over Na2SO4 and concentrated in vacuo. The residue is purified by silica gel chromatography (dichloromethane-methanol, 19:1) to give 4-(5-methoxymethyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-one; MS (ESI) m/z 287.2 (M+H); 1H NMR (400 MHz, MeOD) δ ppm 1.70 (s, 3H), 1.77 (s, 3 H), 3.90 (s, 3 H), 4.39 (s, 2 H), 4.88 (br. s, 1 H), 6.99 (s, 1 H), 7.44-7.53 (m, 1H), 7.56-7.64 (m, 2 H), 7.76 (s, 1 H), 7.86 (d, J=7.6 Hz, 1 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08153674B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-42d2962b92d64e009480798e2fa586b5
Quellennotizuspto-grants-2012_04