関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl chloroformate | HCID 10928 | — |
| 反応物 | 2,3-Lutidine | HCID 11420 | — |
| 反応物 | HCID 178418332 | HCID 178418332 | — |
| 触媒 | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | ethyl 2,3,4-trimethyl-l (4H)-pyridinecarboxylate | HCID 86742392 | — |
反応手順
A solution of 6.75 g of 2,3-lutidine and 475 mg of copper(I) iodide in 150 ml of abs. tetrahydrofuran is cooled to -20° and treated under argon with 3.4 ml of ethyl chloroformate. The reaction mixture is heated to 30° and treated dropwise within 10 minutes with 14 ml of methylmagnesium chloride (3 molar, in tetrahydrofuran). The ethyl 2,3,4-trimethyl-l (4H)-pyridinecarboxylate obtained as the intermediate can be isolated as follows: The reaction mixture is cooled to -10° and treated with 38 ml of aqueous (20%) ammonium chloride solution, whereupon 100 ml of ether are added and the organic solution is washed several times with a 20% ammonium chloride/ammonia (1:1) solution, 2N hydrochloric acid and 10% sodium carbonate solution. The organic solution is dried and concentrated, and the residue is purified on a silica gel column, the medium pressure flash chromatography method (solvent: n-hexane/ether [20:1]) being used and the pressure being produced with nitrogen gas.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04766133 |
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| 出典データセット | uspto-grants-1988_08 |
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| ORD ID | ord-bc2024f6a43d4c4ea3d71242dd15c4d3 |
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| 出典メモ | uspto-grants-1988_08 |
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