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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1061106생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1061106

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Butyl nitriteHCID 10996—
반응물2,3-Dimethyl-4-methylsulfonylbromobenzeneHCID 18757252—
반응물Potassium tert-butoxideHCID 23665647—
용매Acetic AcidHCID 176—
용매DimethylformamideHCID 6228—
생성물3-Bromo-2-methyl-6-methylsulfonylbenzaldoximeHCID 73461944—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06525204B1
출처 데이터셋uspto-grants-2003_02
ORD IDord-f58738cff96c4cd0ae2379cbf83c16ce
출처 메모uspto-grants-2003_02