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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2269677생성일: 2026년 10월 25일

Phosphoric Acid → Ethyl 5,5-dimethyl-3-oxo-octanoate

https://huagongshe.com/reaction/2269677

반응식

참여 물질

역할이름HCID투입량
반응물Phosphoric AcidHCID 1004—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물ImidazolateHCID 3386966—
반응물Potassium ethyl malonateHCID 3446434—
반응물Magnesium ChlorideHCID 5360315—
반응물3,3-dimethylhexanoic AcidHCID 11367061—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 5,5-dimethyl-3-oxo-octanoateHCID 996446171%

반응 단계

Under N2, 1,1′-Carbonyldiimidazole (294 g, 1.82 mol) and THF (1000 mL) was slowly added to 3,3-dimethylhexanoic acid (238 g, 1.65 mol in 200 mL of THF), to a 2 L 3-necked flask. After the addition was completed, the solution was stirred at ambient temperature for 3 hours. Ethyl malonate potassium salt (281 g, 1.65 mol), THF (1500 mL) and magnesium chloride (157 g, 1.65 mol) were added under N2 to a flask equipped with an over-head stirrer. The mixture was stirred at 50° C. for 3 hours. It was then cooled down to room temperature and above acid imidazolide solution was added. The resultant slurry was stirred for 18 hours. H3PO4 (30%, 1.5 L) was added and the mixture was stirred for 1 hour. The aqueous layer was separated and extracted with MTBE (3×700 mL). The combined organic layer was washed with K2CO3 (25%, 2×500 mL) and brine (1000 mL) and dried over magnesium sulfate (˜40 g). The drying reagent was filtered and solvent was removed to give 250 g of ethyl 5,5-dimethyl-3-oxo-octanoate (yield 71%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06329536B1
출처 데이터셋uspto-grants-2001_12
ORD IDord-3c03a68442a645debdc61fe106770e73
출처 메모uspto-grants-2001_12