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Methyl cyanoacetate → Methyl 2-amino-4-(hydroxymethyl)thiophene-3-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl cyanoacetate | HCID 7747 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Propanone, 1-(acetyloxy)-3-chloro- | HCID 38413 | — |
| 反応物 | Sodium sulfide nonahydrate | HCID 73972 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Methyl 2-amino-4-(hydroxymethyl)thiophene-3-carboxylate | HCID 15889790 | 51% |
反応手順
A solution of methyl cyanoacetate (1.18 mL, 13.28 mmol) and sodium sulfide nonahydrate (3.20 g, 13.28 mmol) in methanol (25 mL) at 0° C. was treated with 1-acetoxy-3-chloroacetone (2.0 g, 13.28 mmol). The cold bath was removed and triethylamine (1.86 mL, 13.28 mmol) was added dropwise. The solution was stirred at room temperature for 20 hours then diluted with water and extracted into ethyl acetate. The organic layer was dried over sodium sulfate, filtered, and the solvent removed under vacuum to provide the titled compound (1.25 g, 51%). MS (DCI/NH3) M/Z 188 (M+H)+; 1H NMR (300 MHz, DMSO-d6) δ 3.68 (s, 3 H) 4.45 (dd, J=5.52, 1.47 Hz, 2 H) 4.88 (t, J=5.70 Hz, 1 H) 6.12 (s, 1 H) 7.28 (s, 2 H)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07902203B2 |
| 出典データセット | uspto-grants-2011_03 |
| ORD ID | ord-34d3693602e0460bb323e90f52a7b8b0 |
| 出典メモ | uspto-grants-2011_03 |