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HRID 544380생성일: 2026년 10월 26일

3-Bromo-3-methyl-2-butanone → 2-Methyl-3-oxobutan-2-yl thiocyanate

https://huagongshe.com/reaction/544380

반응식

참여 물질

역할이름HCID투입량
반응물3-Bromo-3-methyl-2-butanoneHCID 344911—
반응물Potassium thiocyanateHCID 516872—
용매AcetoneHCID 180—
생성물2-Methyl-3-oxobutan-2-yl thiocyanateHCID 14195165—

반응 단계

16.5 g (0.1 mol) of 3-bromo-3-methyl-2-butanone and 11.6 g (0.12 mol) of potassium rhodanide in 150 ml of anhydrous acetone are heated at reflux for about 11/2 hours. After cooling, the separated potassium bromide is filtered off under suction and backwashed with a small amount of acetone, and the filtrate is evaporated to dryness at 50° C. under reduced pressure. The residue is dissolved in 200 ml of diethyl ether and the solution is washed three times with 100 ml of water each time, dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure.The crude product is fractionated on a short Vigreux column to yield 3-methyl-3-thiocyanato-2-butanone, b.p. 52° C./0.04 mmHg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04450157
출처 데이터셋uspto-grants-1984_05
ORD IDord-7700561de3e445e3a587857853b19068
출처 메모uspto-grants-1984_05