Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl cyanoacetate → Methyl 2-amino-4-(hydroxymethyl)thiophene-3-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl cyanoacetate | HCID 7747 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Propanone, 1-(acetyloxy)-3-chloro- | HCID 38413 | — |
| 반응물 | Sodium sulfide nonahydrate | HCID 73972 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Methyl 2-amino-4-(hydroxymethyl)thiophene-3-carboxylate | HCID 15889790 | 51% |
반응 단계
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)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07902203B2 |
| 출처 데이터셋 | uspto-grants-2011_03 |
| ORD ID | ord-34d3693602e0460bb323e90f52a7b8b0 |
| 출처 메모 | uspto-grants-2011_03 |