化工社化工社 化学情報印刷レポート · 研究参考用
Sodium Iodide → 3-bromo-6-iodo-4H-thieno[3,2-b]pyrrole-5-carboxylic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | Sodium Sulfite | HCID 24437 | — |
| 反応物 | Chlorosuccinimide | HCID 31398 | — |
| 反応物 | Methyl 3-bromo-4H-thieno[3,2-b]pyrrole-5-carboxylate | HCID 44118324 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 3-bromo-6-iodo-4H-thieno[3,2-b]pyrrole-5-carboxylic acid methyl ester | HCID 58310401 | 68% |
反応手順
To a solution of N-chlorosuccinimide (12 mmol) in acetone (25 mL) was added dropwise a solution of sodium iodide (12 mmol) in acetone (80 mL). 3-Bromo-4H-thieno[3,2-b]pyrrole-5-carboxylic acid methyl ester (10 mmol) in acetone (80 mL) was then added portionwise into the reaction mixture. After 1 hr of stirring, the reaction was poured into a solution of Na2SO3 10% and extracted with AcOEt. Organic phases were washed with brine, dried over Na2SO4, filtered, and evaporated. The residue was purified by silica gel chromatography to give compound 69 as a yellowish solid in 68% yield. 1H NMR (CDCl3, 400 MHz) δ (ppm) 3.96 (s, 3H), 7.26 (s, 1H), 9.22 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09187496B2 |
| 出典データセット | uspto-grants-2015_11 |
| ORD ID | ord-3320e1ee71794558af04f6a3ac3f6a07 |
| 出典メモ | uspto-grants-2015_11 |