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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1627781생성일: 2026년 10월 27일

Hexamethylphosphoramide → Ethyl 2-((2-methyl-1,3-dioxolan-2-yl)methyl)pentanoate

https://huagongshe.com/reaction/1627781

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylphosphoramideHCID 12679—
반응물1-IodopropaneHCID 33643—
반응물Ethyl 2-methyl-1,3-dioxolane-2-propionateHCID 70332—
반응물Lithium diisopropylamineHCID 45051747—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-((2-methyl-1,3-dioxolan-2-yl)methyl)pentanoateHCID 5872530985.1%

반응 단계

To a cooled (−78° C.) solution of lithium diisopropylamine (30 mL; 60 mmol; 2N in THF) in THF (8 mL) was added hexamethylphosphoramide (12 mL) and the solution was stirred for 30 min. A solution of ethyl 3-(2-methyl-1,3-dioxolan-2-yl)propanoate (9.4 g; 50 mmol), in THF (9 mL), was added over 30 min and stirring was continued for 1 h. Propyl iodide (6.84 mL; 70 mmol) was slowly added and the solution was allowed to warm to room temperature for 4 h. the reaction was quenched by adding a saturated aqueous solution of ammonium chloride. The two phases were separated and the aqueous layer was extracted with ethyl acetate (50 mL) and the combined organic layers were dried with sodium sulphatesulphate, filtered and concentrated under reduced pressure. The crude residue was purified by flash-chromatography on silica gel using a gradient of ethyl acetate (0-40%) in heptane to furnish 9.8 g (85%) of ethyl 2-((2-methyl-1,3-dioxolan-2-yl)methyl)pentanoate as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08785638B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-09a1289354ea4c0c82459690074912f1
출처 메모uspto-grants-2014_07