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Pyridine → Carbonic acid chloromethyl ester 2,6-dibromo-4-cyanophenyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Bromoxynil | HCID 15531 | — |
| 反応物 | Chloromethyl chloroformate | HCID 62754 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Carbonic acid chloromethyl ester 2,6-dibromo-4-cyanophenyl ester | HCID 70170999 | 94% |
反応手順
To a suspension of 3,5-dibromo-4-hydroxybenzonitrile (10.0 g, 36.1 mmol) in 180 mL of chloroform was added pyridine (2.92 ml, 36.1 mmol). Chloromethylchloroformate (5.2 mL 60 mmol) was then added over 5 min. The mixture was allowed to stir at room temperature for 12 h. The reaction was then washed with 1% HCl aq, water, and brine. The organic layer was then dried over sodium sulfate, filtered, and evaporated to afford a white solid (12.5 g) in 94% yield. 1H-NMR (300 MHz, CDCl3) δ (ppm): 5.87 (d, 2H), 7.90 (s, 2H). 13C-NMR (300 MHz, CDCl3) δ (ppm): 73.58, 113.87, 115.68, 119.01, 136.40, 149.53, 149.71. Mp=83-85° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06376548B1 |
| 出典データセット | uspto-grants-2002_04 |
| ORD ID | ord-cbf866c32fc24cc9a737db02655fd5d0 |
| 出典メモ | uspto-grants-2002_04 |