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HRID 333077作成日:2026年10月26日

Ethyl Methanesulfonate → Ethyl (diethoxyphosphoryl)methanesulfonate

https://huagongshe.com/reaction/333077

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl MethanesulfonateHCID 6113—
反応物Diethyl chlorophosphateHCID 13139—
反応物n-Butyl lithiumHCID 61028—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl (diethoxyphosphoryl)methanesulfonateHCID 10934205117.1%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08877934B2
出典データセットuspto-grants-2014_11
ORD IDord-40d13101437a4e78a60ba9d76cfe0aff
出典メモuspto-grants-2014_11