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HRID 2049033作成日:2026年10月27日

Hydrochloric Acid → [(alpha-Methyl-4-chlorobenzylidene amino)oxy] acetic acid methyl ester

https://huagongshe.com/reaction/2049033

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物DimethylformamideHCID 6228—
反応物ChloroacetonitrileHCID 7856—
反応物p-Chloroacetophenone oximeHCID 96172—
反応物SodiumHCID 5360545—
反応物(alpha-Methyl-4-chlorobenzylidene amino)oxy acetonitrileHCID 54535538—
溶媒MethanolHCID 887—
溶媒Diisopropyl EtherHCID 7914—
生成物[(alpha-Methyl-4-chlorobenzylidene amino)oxy] acetic acid methyl esterHCID 54127586—

反応手順

Of the (α-methyl-4-chlorobenzylidene amino)oxy acetonitrile (melting point 57° C.-58.5° C.) which was obtained by reacting the sodium salt of 4'-chloroacetophenone oxime, with chloroacetonitrile in dimethylformamide, an amount of 11.3 g was dissolved in diisopropyl ether in which 1.94 g of hydrogen chloride and 1.73 g of methanol had also been dissolved. The solution was diluted with 25 ml of diisopropyl ether and subsequently stirred over night. Then the precipitate was drawn off, washed with absolute ether and dried in a vacuum. The resulting hydrochloride of methyl (α-methyl-4-chlorobenzylidene amino)oxy acetimidate melted at 95° C. with decomposition. After this substance had been dissolved in water, the superscribed ester separated out from the solution. It was extracted with ether and distilled in a vacuum. Boiling point at a pressure of 0.1 mm: 130° C.-132° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04196216
出典データセットuspto-grants-1980_04
ORD IDord-560419011467467dad868d28d2c8f93d
出典メモuspto-grants-1980_04