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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 333077생성일: 2026년 10월 24일

Ethyl Methanesulfonate → Ethyl (diethoxyphosphoryl)methanesulfonate

https://huagongshe.com/ko/reaction/333077

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl MethanesulfonateHCID 6113—
반응물Diethyl chlorophosphateHCID 13139—
반응물n-Butyl lithiumHCID 61028—
용매TetrahydrofuranHCID 8028—
생성물Ethyl (diethoxyphosphoryl)methanesulfonateHCID 10934205117.1%

반응 단계

A solution of ethyl methanesulfonate (4.14 mL, 40.2 mmol) in anhydrous tetrahydrofuran (100 ml) was cooled to −78° C. under a nitrogen atmosphere. N-Butyllithium (20 ml, 50.0 mmol) was added slowly in 7 minutes after which stirring was continued for 15 minutes. Diethyl phosphorochloridate (4.36 mL, 30.2 mmol) was added, the reaction mixture was stirred for 2.5 h, the cooling bath was removed and the mixture was allowed to reach room temperature. The reaction mixture was quenched with aqueous saturated ammonium chloride (150 ml) and the resulting mixture was extracted with EtOAc (2×100 ml). The combined extracts were dried over sodium sulfate and concentrated under reduced pressure to yield 9.20 g of a yellow oil. The oil was purified over silicagel (600 g) using a gradient of ethyl acetate (0-100%) in heptane to yield 1.75 g of the product (6.7 mol, 17%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877934B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-40d13101437a4e78a60ba9d76cfe0aff
출처 메모uspto-grants-2014_11