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HRID 406367作成日:2026年10月24日

Methyl dichlorophosphate → 5-Chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanenitrile

https://huagongshe.com/ja/reaction/406367

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl dichlorophosphateHCID 69611—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物Sodium BicarbonateHCID 516892—
反応物5-Chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanoic acid amideHCID 66618802—
溶媒DichloromethaneHCID 6344—
生成物5-Chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanenitrileHCID 6661893979.6%

反応手順

Methyl dichlorophosphate (1.9 mL) was added dropwise at 20° C. or less to an ice-cooled solution of 5-chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanoic acid amide (3.0 g) and 1,8-diazabicyclo[5,4,0]undec-7-ene (6.4 mL) in methylene chloride (30 mL). After completion of the dropwise addition, the reaction solution was stirred at room temperature for one hour and 25 minutes. A saturated sodium bicarbonate aqueous solution was added to the reaction solution. After stirring for five minutes, the organic layer was separated. The aqueous layer was reextracted with methylene chloride. The combined organic layers were sequentially washed with 1 N hydrochloric acid, water, a saturated sodium bicarbonate aqueous solution and brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (carrier: Wakogel C-200; elution solvent:heptane:ethyl acetate=49:1→19:1) to obtain 2.25 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754100B2
出典データセットuspto-grants-2014_06
ORD IDord-a1c3ad42df04461db79b9e1cc1260091
出典メモuspto-grants-2014_06