참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | 1-Bromo-2-chloro-4-methoxybenzene | HCID 2756863 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 반응물 | 70807-22-6 | HCID 71650496 | — |
| 촉매 | Triphenylphosphine | HCID 11776 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 용매 | Diglyme | HCID 8150 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-(2-Chloro-4-methoxyphenyl)-3-oxobutanenitrile | HCID 22178154 | 801.9% |
반응 단계
Under argon gas atmosphere, to a solution of 1-bromo-2-chloro-4-methoxybenzene (120 g) in a mixed diglyme (230 mL) and 1,2-dimethoxyethane (90 mL), sodium cyano acetone (62.6 g), sodium t-butoxide (114.6 g) and sodium iodide (81.2 g) were added with stirring at room temperature to obtain a suspension. By another process, under argon gas atmosphere, a mixture of diglyme (40 mL), palladium acetate (426 mg) and triphenylphosphine (1.99 g) was stirred for about 30 minutes at 110° C. to dissolve. This solution was dropped into the above suspension. The mixture was warmed to 110 to 115° C. of internal temperature and stirred for 7 hours. The reaction mixture was cooled, diluted with ethyl acetate (480 mL) and washed with an aqueous solution of sulfuric acid (concentrated sulfuric acid 101 g/water 660 mL). The organic layer was washed with 10% saturated aqueous solution of sodium chloride (360 mL) twice. Activated charcoal (3.6 g) was added to the organic layer. The mixture was stirred for 1 hour and filtered. The filtrate was washed with ethyl acetate (240 mL) to obtain a solution of 1-cyano-1-(2-chloro-4-methoxyphenyl)propan-2-on (971.7 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07947697B1 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
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| ORD ID | ord-81c0bcd4bf2d48be9d8504a41b7fcc44 |
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| 출처 메모 | uspto-grants-2011_05 |
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