戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 5595作成日:2026年10月24日

Benzyl Chloride → 1-Benzyl-2-phenyl-1H-indole

https://huagongshe.com/ja/reaction/5595

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl ChlorideHCID 7503—
反応物2-PhenylindoleHCID 13698—
反応物Potassium HydroxideHCID 14797—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物1-Benzyl-2-phenyl-1H-indoleHCID 1174804413.2%

反応手順

A mixture of 19.33 g (0.1 mole) of 2-phenylindole, 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 55°-60° for 24 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 with 2N HCl (2×50 mL), H2O (2×50 mL), and 50 mL of brine and dried over MgSO4. Evaporation of the solvent left 32.3 g of dark brown oil. The oil was chromatographed on a 1100 g column of silica gel. The column was elut4d 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 18-20 were combined giving 3.74 g (13%) of 1-benzyl-2-phenylindole as a solid.

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-3ef121dbf1f0400b85825dd9302cc9ce
出典メモuspto-grants-1993_09