참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | 2,4-Dichloronitrobenzene | HCID 11899 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Methyl 2-hydroxy-5-methoxybenzoate | HCID 4072341 | — |
| 촉매 | Copper | HCID 23978 | — |
| 촉매 | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(5-Chloro-2-nitrophenoxy)-5-methoxybenzoic acid, methyl ester | HCID 13689096 | — |
반응 단계
To a solution of 61.8 g of 2-hydroxy-5-methoxybenzoic acid, methyl ester in 700 ml DMF was added 14.96 g of a 60% suspension of sodium hydride in mineral oil. This was followed by addition of 50.88 g of sodium iodide, 64.64 g of copper(I)iodide, and 2.16 g of finely powdered copper metal. The mixture was heated to 85° C., for 15 minutes, then 71.7 g of 2,4-dichloronitrobenzene was added, and the reaction was stirred at 85° C. for 16 hours. The mixture was filtered, and the filtrate concentrated to an oily residue. Sodium thiosulfate, 400 ml of a 20% solution was added, followed by extraction with ethyl acetate (3×400 ml). The combined ethyl acetate extracts were washed with water (2×325 ml), dried over anhydrous sodium sulfate, then evaporated to afford a pale yellow solid, which was triturated with cyclohexane and filtered giving the title compound, mp 114°-116° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04604390 |
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| 출처 데이터셋 | uspto-grants-1986_08 |
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| ORD ID | ord-b096b84c5f1f40f39666b10f5de8f91b |
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| 출처 메모 | uspto-grants-1986_08 |
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