化工社化工社 化学情報印刷レポート · 研究参考用
4-Acetylbenzoic Acid → 4-(2-Amino-1,3-thiazol-4-yl)benzoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Acetylbenzoic Acid | HCID 11470 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | Carbonyl bromide | HCID 79057 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | Thiourea | HCID 2723790 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-(2-Amino-1,3-thiazol-4-yl)benzoic acid | HCID 613179 | — |
反応手順
A solution of 4-acetyl-benzoic acid (10 g, 61 mmol), in HOAc (400 mL) at 55° C. was treated with bromine (1 eq., 3.12 mL) dropwise over 10 minutes. After 90 minutes the reaction was cooled, the acetic acid was removed, ethyl acetate (50 mL) was added and then removed to get rid of the remainder of the acetic acid. The crude bromo ketone was then dissolved in ethanol (200 mL) with NaOAc (12 g) and thiourea (1 eq. 4.4 g) was added. The suspension was stirred at room temperature for 15 hours. The solvents were removed and the solids washed with water (3×100 mL) then ether:ethanol (4:1, 3×100 mL) and dried to give the product as a tan solid. MS: 221.2 (M+H+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07595398B2 |
| 出典データセット | uspto-grants-2009_09 |
| ORD ID | ord-d29e033db8d04bd3b35694af9be5cf39 |
| 出典メモ | uspto-grants-2009_09 |