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HRID 51465作成日:2026年10月24日

Benzenepropanal → 3-Phenylmethyl-7-methoxyindole

https://huagongshe.com/ja/reaction/51465

反応式

関与物質

役割名称HCID仕込み量
反応物BenzenepropanalHCID 7707—
反応物Phosphorus trichlorideHCID 24387—
反応物Sodium BicarbonateHCID 516892—
反応物2-Methoxyphenylhydrazine HydrochlorideHCID 2849445—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物3-Phenylmethyl-7-methoxyindoleHCID 22740738—

反応手順

A mixture of 15 gm (0.086 mol) of 2-methoxyphenylhydrazine hydrochloride and 12 mL (0.09 mol) of 3-phenylpropionaldehyde in 300 mL of toluene was refluxed for 1.5 hours with azeotropic removal of water. The suspension was cooled, evaporated in vacuo and the residue dissolved in 500 mL of dichloromethane and stirred with 9 mL (0.09 mol) of phosphorous trichloride for 18 hours. The solution was poured into ice-water, stirred well, and made basic with sodium bicarbonate. The organic phase was washed with saturated sodium chloride, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel eluting with a gradient hexane/5-15% ethyl ether to give product, 8.0 gm, 40%, as a viscous oil. 1H NMR (CDCl3) δ: 3.95 (s, 3H), 4.10 (s, 2H), 6.65 (d, 1H), 6.90 (s, 1H), 7.00 (t, 1H), 7.10 (d, 1H), 7.20 (m, 1H), 7.30 (m, 4H), 8.20 (br s, 1H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713645B1
出典データセットuspto-grants-2004_03
ORD IDord-e5b31f1a44974878a00a6afaac8c47d2
出典メモuspto-grants-2004_03