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HRID 27423作成日:2026年10月25日

Water → 2-(alpha-Ethoxycarbonyl-4-chlorobenzylidene)-1-methylperhydroazepine

https://huagongshe.com/reaction/27423

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl (4-chlorophenyl)acetateHCID 84177—
反応物SodiumHCID 5360545—
反応物HCID 178483040HCID 178483040—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
生成物2-(alpha-Ethoxycarbonyl-4-chlorobenzylidene)-1-methylperhydroazepineHCID 53941548—

反応手順

Add (drop by drop at 90° in a stream of nitrogen to let the alcohol escape) a solution of 4.6 g of sodium in 100 ml of ethyl alcohol to a mixture of 53.2 g of the title compound of Example 1 and 29.8 g of ethyl 4-chlorophenylacetate. Stir it for a further 4 hours at 90° and then cool it to ambient temperature. Mix the cooled reaction mixture with 100 ml of water and 100 ml of diethyl ether, collect the organic phase and dry the latter over sodium sulfate. Concentrate the dried organic phase and then distil off any excess ethyl 4-chlorophenylacetate under a high vacuum to obtain a crude yield [15.5 g (34% of theory)] of the title compound as yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04221788
出典データセットuspto-grants-1980_09
ORD IDord-ca593dee24784df38759aae09bcc0859
出典メモuspto-grants-1980_09