関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | Triethyl 1,6-dihydro-6-oxo-2,3,5-pyridinetricarboxylate | HCID 19958207 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Triethyl 6-chloro-2,3,5-pyridinetricarboxylate | HCID 19958209 | 47% |
反応手順
A solution of triethyl 1,6-dihydro-6-oxo-2,3,5-pyridine-tricarboxylate (39.7 g) in 300 mL of phosphorous oxychloride and 0.5 mL dimethylformamide is stirred at 100° C. for four hours and 15 minutes. After cooling, the excess phosphorous oxychloride is removed under vacuum. The residue is taken up in 200 mL methylene chloride and the solution poured into 500 mL of ice water and the layers are separated. The aqueous layer, made basic with concentrated ammonium hydroxide and ice, is extracted with 150 mL methylene chloride. The combined methylene chloride extracts are dried over magnesium sulfate, filtered and concentrated under vacuum, and the resulting crude product is chromatographed on silica using 5:1 hexanes:ethyl acetate and then 4:1 hexanes:ethyl acetate as eluants affording 26.5 g (47%) of the title product as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05252538 |
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| 出典データセット | uspto-grants-1993_10 |
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| ORD ID | ord-6a1bc078aeba4bac86d32e1edec39aac |
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| 出典メモ | uspto-grants-1993_10 |
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