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HRID 1706873作成日:2026年10月26日

Potassium diethyl dithiophosphate → O,O-diethyl S-(4-chloro-5-methyl-3-oxo-4-isoxazolin-2-ylmethyl) phosphorodithioate

https://huagongshe.com/reaction/1706873

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium diethyl dithiophosphateHCID 11481509—
反応物4-Chloro-2-chloromethyl-5-methyl-4-isoxazolin-3-oneHCID 20332913—
生成物O,O-diethyl S-(4-chloro-5-methyl-3-oxo-4-isoxazolin-2-ylmethyl) phosphorodithioateHCID 2033290485.8%

反応手順

To the solution obtained in step (b) above was added dropwise the isoxazolinone solution obtained in step (a) above, with stirring, over a period of 5 minutes at ambient temperature. The mixture was then stirred for a further 30 minutes, also at ambient temperature. After distilling off the solvent, 100 ml of benzene and 25 ml of water were added to the residue and the benzene phase was washed, in turn, with 25 ml of a 5% w/w aqueous sodium bicarbonate solution and twice with 100 ml of a saturated aqueous sodium chloride solution. The benzene solution was then dried over anhydrous sodium sulphate and the solvent was distilled off. The residue was then purified as described in step (b) of Example 3, affording 28.5 g (85.8% of theory) of O,O-diethyl S-(4-chloro-5-methyl-3-oxo-4-isoxazolin-2-ylmethyl) phosphorodithioate, in the form of a yellow oil, n20D =1.5457.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04209512
出典データセットuspto-grants-1980_06
ORD IDord-546122d1393b4150ae546dc80676e946
出典メモuspto-grants-1980_06