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HRID 1109169作成日:2026年10月25日

Iodoacetamide → 1,3,4,5-tetrahydro-6-methoxy-2H-benzo[e]indol-2-one

https://huagongshe.com/reaction/1109169

反応式

関与物質

役割名称HCID仕込み量
反応物IodoacetamideHCID 3727—
反応物PyrrolidineHCID 31268—
反応物5-Methoxy-2-tetraloneHCID 259194—
触媒p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物1,3,4,5-tetrahydro-6-methoxy-2H-benzo[e]indol-2-oneHCID 1902147589%

反応手順

439 g (2.49 mol) of 5-methoxy-2-tetralone and 227 ml (3.67 mol) of pyrrolidine were dissolved in 3 l of toluene. After the addition of 16.4 g (0.09 mol) of p-toluenesulfonic acid monohydrate the mixture was boiled for 4 hours, whereby the resulting water was removed continuously using a water separator. Thereupon, the toluene was distilled off in a vacuum. The residue was dissolved in 1 l of tetrahydrofuran, whereupon a solution of 500 g (2.70 mol) of iodoacetamide in 2.5 l of tetrahydrofuran was added dropwise at room temperature. The mixture was boiled at reflux for 30 minutes, then cooled to room temperature and stirred for a further 12 hours. The solid was filtered off and washed with tetrahydrofuran. There were obtained 475 g (89%) of 1,3,4,5-tetrahydro-6-methoxy-2H-benzo[e]indol-2-one as white crystals with m.p. 220°-222°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05318967
出典データセットuspto-grants-1994_06
ORD IDord-42f005d01a904aca95cd01e5feedb0de
出典メモuspto-grants-1994_06