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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1667359생성일: 2026년 10월 26일

Ethyl 2-methylacetoacetate → 5-Ethyloxycarbonyl-5-methyl-6-oxo-1-heptanesulfonic acid

https://huagongshe.com/reaction/1667359

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 2-methylacetoacetateHCID 701—
반응물1,4-Butane sultoneHCID 15411—
반응물Sodium hydrideHCID 24758—
용매DimethylformamideHCID 6228—
생성물5-Ethyloxycarbonyl-5-methyl-6-oxo-1-heptanesulfonic acidHCID 58084006122.6%

반응 단계

Ethyl 2-methylacetoacetate (43.2 g) in N,N-dimethylformamide (25 ml) was added to a suspension of sodium hydride (12.0 g of 60% NaH in mineral oil) in N,N-dimethylformamide (100 ml), dropwise with ice-bath cooling. This mixture was allowed to warm to ambient temperature for 30 mins before re-cooling. 1,4-butanesultone (40.8 g) in N,N-dimethylformamide (25 ml) was then added dropwise. The final mixture was heated at 50° C. for 18 hrs, then quenched with 50 ml of water. The solvent was evaporated under vacuum; the residue was partitioned between water and diethyl ether. The aqueous layer was collected, washed with fresh diethyl ether and evaporated under vacuum; final drying was under high vacuum over phosphorus pentoxide. A yield of 103 g of 5-(ethoxycarbonyl)-5-methyl-6-oxoheptane-1-sulfonic acid was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08044203B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-a84c320341604e82bcceda72e086f20b
출처 메모uspto-grants-2011_10