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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40427생성일: 2026년 10월 23일

Hydrochloric Acid → 5-Methyl-6-oxoheptanesulfonic acid

https://huagongshe.com/ko/reaction/40427

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl 2-methylacetoacetateHCID 701—
반응물Sodium HydroxideHCID 14798—
반응물1,4-Butane sultoneHCID 15411—
반응물Sodium hydrideHCID 24758—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물5-Methyl-6-oxoheptanesulfonic acidHCID 57903351—

반응 단계

Ethyl 2-methylacetoacetate (50 g) in DMF (25 ml) was added to a suspension of sodium hydride (12.0 g of 60% NaH in mineral oil) in DMF (100 ml), dropwise with ice-bath cooling over 1 hour, (internal temperature 0-4° C.). This mixture was allowed to warm to ambient temperature for 45 mins with stirring before re-cooling. A solution of 1,4-butanesultone (45 g) in DMF (25 ml) was then added dropwise over 15 minutes. The final mixture was heated at 60° C. for 18 hours. The solvent was removed by rotary evaporation and the residue partitioned between water and diethyl ether. The aqueous layer was collected, washed with fresh diethyl ether and rotary evaporated to yield a sticky foam. This intermediate was dissolved in water (100 ml) and sodium hydroxide (17.8 g) added over 15 minutes with stirring. The mixture was heated at 90° C. for 18 hours. The cooled reaction mixture was adjusted to ˜pH2 by the addition of concentrated hydrochloric acid (˜40 ml). The solution was rotary evaporated and dried under vacuum. The yellow solid was washed with ethanol containing 2% hydrochloric acid (3×150 ml). The ethanolic solution was filtered, rotary evaporated and dried under vacuum to yield a yellow solid. Yield 70 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08529874B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-dc1b563f1b5047ec897e3bd65136287a
출처 메모uspto-grants-2013_09