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HRID 484249作成日:2026年10月23日

p-Toluenesulfonic acid → 1-Methyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-aceticacid, ethyl ester

https://huagongshe.com/ja/reaction/484249

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 AcetoacetateHCID 8868—
反応物5-Benzyloxy-3-(2-hydroxyethyl)indoleHCID 744849—
溶媒BenzeneHCID 241—
生成物1-Methyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-aceticacid, ethyl esterHCID 13171802985.3%

反応手順

A mixture consisting of 5-benzyloxytryptophol (4.5 g, 0.017 mol), benzene (200 mL), ethyl acetoacetate (3.4 g, 0.026 mol) and p-toluenesulfonic acid (0.5 g) is refluxed for 2.5 hours using a Dean-stock trap to remove the water. The reaction mixture is cooled to room temperature and washed with 5% sodium bicarbonate, (1×200 mL), water (200 mL) and brine (100 mL), dried (MgSO4), filtered and concentrated to give 8.0 g of crude product as a thick oil, which is flash chromatographed on silica gel using 20% ethyl acetate/hexane as an eluent to afford 5.5 g oil which solidifies upon standing, m.p. 96°-98° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05229516
出典データセットuspto-grants-1993_07
ORD IDord-81281567c4c44990919e4c9f2a565b1f
出典メモuspto-grants-1993_07