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HRID 238930作成日:2026年10月26日

Hydroxyamine hydrochloride → N-{4-[1-(hydroxyamino)ethylidene]cyclohexa-2,5-dien-1-ylidene}methanesulfonamide

https://huagongshe.com/reaction/238930

反応式

関与物質

役割名称HCID仕込み量
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物N-(4-acetylphenyl)methanesulfonamideHCID 684083—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物N-{4-[1-(hydroxyamino)ethylidene]cyclohexa-2,5-dien-1-ylidene}methanesulfonamideHCID 6612326—

反応条件

温度70 °C

反応手順

A mixture of 4′-(Methylsulfonylamino)acetophenone (13-5, 5 mmol) and hydroxylamine hydrochloride (0.695 g, 10 mmol) in pyridine (5 mL) was heated at 70° C. for 3 h. The reaction mixture was cooled to room temperature, diluted with H2O, and extracted with EtOAc several times. The combined organic layers were washed with H2O and brine, dried over MgSO4, filtered, and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexanes (1:1) as eluant to 4′-Methylsulfonylamino)acetophenone oxime (13-8, LJO-299).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642657B2
出典データセットuspto-grants-2014_02
ORD IDord-8be3c1feb80d41cca7259ae6441eb595
出典メモuspto-grants-2014_02