戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 554689作成日:2026年10月25日

Water → 3-Bromo-2-methyl-6-methylsulfonylbenzaldoxime

https://huagongshe.com/reaction/554689

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Butyl nitriteHCID 10996—
反応物2,3-Dimethyl-4-methylsulfonylbromobenzeneHCID 18757252—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Acetic AcidHCID 176—
溶媒DimethylformamideHCID 6228—
生成物3-Bromo-2-methyl-6-methylsulfonylbenzaldoximeHCID 73461944—

反応手順

A solution of 2.1 g (20 mmol) of n-butyl nitrite (97%) and 4 g (15 mmol) of 2,3-dimethyl-4-methylsulfonylbromobenzene in 50 ml of dimethylformamide is cooled to from −55 to −60° C., and a solution of 2.8 g (25 mmol) of potassium tert-butoxide in 35 ml of dimethylformamide is added dropwise at this temperature, over a period of 20 minutes. The reaction is monitored by HPLC. For work-up, initially 10 ml of water are added, and the mixture is then adjusted to pH 5-6 using about 9 ml of glacial acetic acid. The mixture is then poured onto 100 ml of ice-water and the aqueous phase is extracted with methylene chloride. The organic phase is washed with sodium bicarbonate solution, dried over magnesium sulfate and concentrated. This gives 3.6 g of an oily crude product (90% by HPLC) which can be purified by recrystallization from toluene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08049017B2
出典データセットuspto-grants-2011_11
ORD IDord-3587f9d2a47c4b4fb37857e5828c0e5b
出典メモuspto-grants-2011_11