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HRID 2233741作成日:2026年10月25日

1-(4-Chlorophenoxy)acetone → 7-Bromo-3-(4-chlorophenoxy)-2-methyl-4-nitro-1H-indole

https://huagongshe.com/reaction/2233741

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Chlorophenoxy)acetoneHCID 239874—
反応物(2-Bromo-5-nitrophenyl)hydrazineHCID 53402499—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物7-Bromo-3-(4-chlorophenoxy)-2-methyl-4-nitro-1H-indoleHCID 68617744—

反応条件

温度75 °C

反応手順

A mixture of the compound from (i) (2.4 g) and 1-(4-Chloro-phenoxy)-propan-2-one (1.65 g) in MeCN (20 ml) and water (5 ml) was stirred for 16 h. The volatiles were removed in vacuo. AcOH (50 ml) was added and the reaction heated at 75° C. for 72 h. The volatiles were evaporated under reduced pressure and the residue was purified by chromatography on silica eluting with 5% ethylacetate/iso-hexane. Yield 0.34 g

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07709521B2
出典データセットuspto-grants-2010_05
ORD IDord-bd892b9f6f3440b48b6590ad1fbadcc5
出典メモuspto-grants-2010_05