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Ethyl chloroformate → Ethyl 3-bromo-5-chloropyridine-4-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl chloroformate | HCID 10928 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 3-Bromo-5-chloropyridine | HCID 606256 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Ethyl 3-bromo-5-chloropyridine-4-carboxylate | HCID 46311456 | 81.4% |
反応手順
3-bromo-5-chloropyridine (25 g, 130 mmol) in THF (50 mL) was added slowly to a solution of LDA (140 mmol) in THF (250 mL) at −78° C. over 10 minutes. After stirring for 30 minutes, ethyl chloroformate (26 mL, 260 mmol) in THF (30 mL) was added in portions over 5 minutes. After 10 more minutes, the reaction mixture was poured into cold 10% aqueous NaHCO3 (500 mL). The mixture was extracted with ethyl acetate (2×250 mL). The organic layer was dried over MgSO4 and evaporated. The crude solid was filtered through a silica pad with hexane (500 mL). The filtrate was evaporated to provide pure ethyl 3-bromo-5-chloropyridine-4-carboxylate (28 g, 80% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09040538B2 |
| 出典データセット | uspto-grants-2015_05 |
| ORD ID | ord-a24bf4213c4647b2831f5ff0ee2caa8f |
| 出典メモ | uspto-grants-2015_05 |