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HRID 55931作成日:2026年10月26日

1-Naphthoic acid → (2-Methyl-1H-indol-3-yl)(naphthalen-1-yl)methanone

https://huagongshe.com/reaction/55931

反応式

関与物質

役割名称HCID仕込み量
反応物1-Naphthoic acidHCID 6847—
反応物3-NaphthoylindoleHCID 10355825—
反応物HCID 178418689HCID 178418689—
溶媒Diethyl EtherHCID 3283—
溶媒Thionyl ChlorideHCID 24386—
生成物(2-Methyl-1H-indol-3-yl)(naphthalen-1-yl)methanoneHCID 117786841,133.2%

反応条件

温度0 °C

反応手順

2-Methylindole 1 (10 g, 76 3 mmol) was dissolved in diethylether (100 ml) under nitrogen atmosphere and cooled to 0° C. MeMgBr (3M) solution (26.7 ml, 80.15 mmol) was added dropwise and allowed to stir at room temperature for 3 hours. In the meantime, 1-naphthoic acid (13.13 g, 76 3 mmol) was dissolved in thionyl chloride (50 ml) and refluxed for 90 min, then the solvent was removed under vacuo and the residue was dissolved in diethylether (50 ml). The resulting solution was added dropwise to the indole reaction mixture at 0° C. and then allowed to stir at room temperature for 2 hours. A solution of ammonium chloride (200 ml) was added to the reaction mixture and the resulting mixture was stirred at room temperature overnight. The solid that was formed was collected by filtration, washed with water and hexane then dried in a dessicator over phosphorous pentoxide to give 9.7 g (45%) (2-methyl-1H-indol-3-yl)(naphthalen-1-yl) methanone 2 as a cream solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434687B2
出典データセットuspto-grants-2016_09
ORD IDord-ba58fb38ded749dba9c0682a8cc39af9
出典メモuspto-grants-2016_09