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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 406367생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Methyl dichlorophosphateHCID 69611—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Sodium BicarbonateHCID 516892—
반응물5-Chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanoic acid amideHCID 66618802—
용매DichloromethaneHCID 6344—
생성물5-Chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanenitrileHCID 6661893979.6%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754100B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-a1c3ad42df04461db79b9e1cc1260091
출처 메모uspto-grants-2014_06