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HRID 414825作成日:2026年10月26日

Water → 1-(3,4-Dichlorophenoxy)-7,8-dimethoxy-2,3,4,5-tetrahydro-3-benzazepine oxalate

https://huagongshe.com/reaction/414825

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物DimethylformamideHCID 6228—
反応物Sodium hydrideHCID 24758—
反応物1,2-Dichloro-4-fluorobenzeneHCID 74028—
反応物HCID 13118512HCID 13118512—
生成物1-(3,4-Dichlorophenoxy)-7,8-dimethoxy-2,3,4,5-tetrahydro-3-benzazepine oxalateHCID 1434911357%

反応条件

温度60 °C

反応手順

A solution of 7,8-dimethoxy-1-hydroxy-2,3,4,5-tetrahydro-3-benzazepine (3 g, 13.4 mmole) in 25 ml dimethylformamide was slowly dropped into a stirring suspension of sodium hydride (50% oil dispersion, 0.7 g, 14.8 mmole), previously washed with hexane, in 10 ml dimethylformamide. After the addition was completed, the mixture was warmed for one hour at 60° C., then was cooled and a solution of 3,4-dichlorofluorobenzene (2.4 g, 14.8 mmole) in 10 ml dimethylformamide was added. After stirring two hours at ambient temperature, the reaction mixture was stirred with 400 ml water and was extracted with ethyl acetate. The organic extract was washed with ethyl acetate. The organic extract was washed with water and saturated NaCl and was dried (anhydrous MgSO4), filtered and evaporated to 7 g of an oil. This oil was purified by HPLC (silica gel, 5% methanol in dichloromethane) to give 2.8 g (57%) of an oil. This oil was converted to the oxalate salt as in Example 1 and was recrystallized from ethyl acetate-methanol to give 2.1 g (34%) of 1,(3-4-dichlorophenoxy)-7,8-dimethoxy-2,3,4,5-tetrahydro-3-benzazepine oxalate, d 167°-168° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04794181
出典データセットuspto-grants-1988_12
ORD IDord-ec49c880435b4f18b7729301aa2b6e48
出典メモuspto-grants-1988_12