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HRID 614719作成日:2026年10月26日

4-(Chloromethyl)-2-nitroanisole → Benzenemethanaminium, N,N-bis[3-(formylamino)propyl]-4-methoxy-N-methyl-3-nitro-, chloride (1:1)

https://huagongshe.com/reaction/614719

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Chloromethyl)-2-nitroanisoleHCID 80785—
反応物Formamide, N,N'-[(methylimino)di-3,1-propanediyl]bis-HCID 3084810—
溶媒AcetonitrileHCID 6342—
生成物Benzenemethanaminium, N,N-bis[3-(formylamino)propyl]-4-methoxy-N-methyl-3-nitro-, chloride (1:1)HCID 100848—

反応手順

A mixture of 54.0 parts of N,N-bis(3-formamidopropyl)methylamine, 50.4 parts of 4-methoxy-3-nitrobenzyl chloride, and 78 parts of acetonitrile was stirred at reflux for seven and a half hours. An additional 78 parts of acetonitrile was added to the reaction mixture causing an oil to separate. Heating at reflux was continued for an additional two hours and the 140 parts of acetonitrile was distilled away and 200 parts of water was added. The remaining acetonitrile was removed by distillation and the cooled reaction mixture was filtered with the aid of diatomaceous earth to obtain an aqueous solution of N-methyl-N-(3-nitro-4-methoxybenzyl)-N,N-bis(3-formamidopropyl)ammonium chloride. The solution was used directly for reduction of the nitro group.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04146558
出典データセットuspto-grants-1979_03
ORD IDord-11dae8c88a7c43f6b169a6776e6708a0
出典メモuspto-grants-1979_03