참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl dichlorophosphate | HCID 69611 | — |
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 5-Chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanoic acid amide | HCID 66618802 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-Chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanenitrile | HCID 66618939 | 79.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08754100B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-a1c3ad42df04461db79b9e1cc1260091 |
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| 출처 메모 | uspto-grants-2014_06 |
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