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HRID 37705作成日:2026年10月23日

p-Toluenesulfonic acid → 1,3,4,9-Tetrahydro-1,1-diethyl-6-(phenylmethoxy)pyrano[3,4-b]indole

https://huagongshe.com/ja/reaction/37705

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Ethyl ketoneHCID 7288—
反応物5-Benzyloxy-3-(2-hydroxyethyl)indoleHCID 744849—
溶媒BenzeneHCID 241—
生成物1,3,4,9-Tetrahydro-1,1-diethyl-6-(phenylmethoxy)pyrano[3,4-b]indoleHCID 19935702—

反応手順

A mixture consisting of 5-benzyloxytryptophol (7.0 g, 0.0262 mol), diethyl ketone (10 mL), benzene (400 mL) and p-toluene sulfonic acid is refluxed for 3.5 hours using a Dean-Stark tap to remove the water. The reaction mixture is cooled to room temperature, washed with 5% sodium bicarbonate, water (200 mL), brine (200 mL), dried (MgSO4), filtered and concentrated to give 9.9 g of crude product. The crude product is flash chromatographed on silica gel using 15% ethyl acetate/hexane as an eluent to afford 6.5 g of pure title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420289
出典データセットuspto-grants-1995_05
ORD IDord-a09d1d9c3a1d4cbca6ef532f7dd1bb33
出典メモuspto-grants-1995_05