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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium diethyl dithiophosphate | HCID 11481509 | — |
| 反応物 | 4-Chloro-2-chloromethyl-5-methyl-4-isoxazolin-3-one | HCID 20332913 | — |
| 生成物 | O,O-diethyl S-(4-chloro-5-methyl-3-oxo-4-isoxazolin-2-ylmethyl) phosphorodithioate | HCID 20332904 | 85.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04209512 |
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| 出典データセット | uspto-grants-1980_06 |
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| ORD ID | ord-546122d1393b4150ae546dc80676e946 |
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| 出典メモ | uspto-grants-1980_06 |
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