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HRID 983521作成日:2026年10月24日

Ammonium Chloride → 3,5-Dichloro-3-(2,3-dimethoxyphenyl)-1,3-dihydro-2h-indol-2-one

https://huagongshe.com/ja/reaction/983521

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物tert-butyl N-(4-chlorophenyl)carbamateHCID 546372—
反応物Ethyl 2-(2,3-dimethoxyphenyl)-2-oxoacetateHCID 21905960—
反応物HCID 178418306HCID 178418306—
溶媒Diethyl EtherHCID 3283—
溶媒PentaneHCID 8003—
溶媒TetrahydrofuranHCID 8028—
生成物3,5-Dichloro-3-(2,3-dimethoxyphenyl)-1,3-dihydro-2h-indol-2-oneHCID 21905931—

反応条件

温度-40 °C

反応手順

A mixture of 11.4 g of tert-butyl 4-chlorophenylcarbamate in 100 ml of ether is cooled to −40° C. under an atmosphere of dry nitrogen, 80 ml of a 1.5 M solution of tert-butyllithium in pentane are added dropwise and the mixture is left stirring at −20° C. for 3 hours. The reaction mixture is cooled to −40° C., a solution-of 14 g of the compound obtained in step A in 50 ml of THF is added over 1 hour and the mixture is left stirring for 4 days at RT. The reaction mixture is poured into saturated NH4Cl solution and the precipitate formed is spin-filtered off and dried. 10.2 g of the expected product are obtained and are used without further purification in the following step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06864277B2
出典データセットuspto-grants-2005_03
ORD IDord-5e48b884da0a4dc68bc38430fdae107f
出典メモuspto-grants-2005_03