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HRID 353030作成日:2026年10月24日

Methyl iodide → 2,3,4,5-tetramethoxytoluene

https://huagongshe.com/ja/reaction/353030

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N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物HexaneHCID 8058—
反応物1,2,3,4-TetramethoxybenzeneHCID 607773—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2,3,4,5-tetramethoxytolueneHCID 987776484%

反応条件

温度0 °C

反応手順

Syper, L. et al., Tetrahedron 36:123 (1980). To a solution of 1,2,3,4-tetramethoxybenzene 12 (4.0 g, 20.2 mmol) and TMEDA (6 mL, 38.0 mmol) in hexanes (44 mL) and THF (80 mL) at 0° C. under Ar, n-BuLi in hexane (1.6 M, 25.6 mmol) was added dropwise over a 10 min period and the reaction stirred for 30 min at 0° C. under Ar. Subsequent to dropwise addition of CH3I (20 mL, 160 mmol) over an 8 min period, the reaction was stirred for 3 h at 0° C. under Ar and then quenched by addition of aqueous NH4Cl and ether (20 mL). The organic layer was sequentially washed with concentrated NH4OH, water, and brine. Drying and concentration of the organic layer was followed by purification of the residue by flash chromatography (hexanes, hexanes/EtOAc, 19:1, v/v) to afford 13 as a clear oil (3.6 g, 83%). 1H NMR (CDCl3): δ6.45 (s, 1 H), 3.93 (s, 3 H), 3.87 (s, 3 H), 3.82 (s, 3 H), 3.79 (s, 3 H), 2.23 (s, 3 H). 13C NMR (CDCl3): δ149.0, 146.9, 145.3, 140.7, 125.7, 108.2, 61.0, 60.9, 60.5, 55.9, 15.7.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06750049B1
出典データセットuspto-grants-2004_06
ORD IDord-3f2644736c3c4aa6917f6ae72bb49d96
出典メモuspto-grants-2004_06