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HRID 5597作成日:2026年10月23日

2-Methylindole → 1-Benzyl-2-methylindole

https://huagongshe.com/ja/reaction/5597

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethylindoleHCID 7224—
反応物Benzyl ChlorideHCID 7503—
反応物Potassium HydroxideHCID 14797—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物1-Benzyl-2-methylindoleHCID 33071519.4%

反応手順

A mixture of 13.11 g (0.1 mole) of 2-methylindole, 13.92 g (0.11 mole) of benzyl chloride, 33 g (0.5 mole) of 85% KOH, 14 mL of H2O, 2.5 g (2.5 mmoles) of PEG-1000, and 100 mL of toluene was stirred and heated at 60° for 23 hours. After cooling to room temperature, 100 mL of H2O was added. The layers were separated. The aqueous layer was extracted with 100 mL of toluene. The combined toluene phases were washed 2N HCl (2×50 mL), H2O (2×50 mL), and 50 mL of brine and dried over MgSO4. Evaporation of the solvent left 26.98 g of dark brown oil. The oil was chromatographed on a 1100 g column of silica gel. The column was eluted with 25% CH2Cl2 -Skellysolve B and 200 mL fractions were collected. The fractions were assayed by silica gel tlc (1×4") (25% CH2Cl2 -Skellysolve B). Fractions 20-22 were combined giving 2.08 g (9%) of 1-benzyl-2-methylindole as a yellow oil which solidified.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05245046
出典データセットuspto-grants-1993_09
ORD IDord-1e9c28188ba44ba1b3e90f556b1d3cd8
出典メモuspto-grants-1993_09