戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 727494作成日:2026年10月26日

Diethyl chlorophosphate → Isopropyl (Diethoxyphosphoryl)methanesulfonate

https://huagongshe.com/reaction/727494

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl chlorophosphateHCID 13139—
反応物Isopropyl methanesulfonateHCID 13551—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Isopropyl (Diethoxyphosphoryl)methanesulfonateHCID 1572597567%

反応条件

温度-40 °C

反応手順

To a rapidly stirred solution of 8.28 g (60 mmol) of isopropyl methanesulfonate in 150 mL of THF at -73° C. (internal temp.) was added 25 mL (60 mmol) of 2.4M n-butyllithium dropwise over 20 min. The internal temperature was not allowed to rise above -69° C. throughout the course of the addition. After an additional 15 min., 5.17 g (30 mmol) of freshly distilled diethyl chlorophosphate was added at a rate to keep the solution temperature below -69° C. The reaction mixture was stirred for 0.3 h at -73° C. and for 0.5 h at -40° C. when it was quenched with 125 mL of saturated NH4Cl solution. The reaction mass was warmed to room temperature and the THF removed under reduced pressure. The remainder was partitioned between methylene chloride and water (3×75 mL). The extracts were dried (Na2SO4), concentrated, and purified by flash chromatography (350 g silica gel) eluting with 1:1 methylene chloride/ether to provide 5.20 g (67%) of title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05712396
出典データセットuspto-grants-1998_01
ORD IDord-595cfc84a1e44c3f97b7e9e63e460877
出典メモuspto-grants-1998_01