Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanol → 2-Methoxythiophene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Sodium Cyanide | HCID 8929 | — |
| 반응물 | 2-Bromothiophene | HCID 13851 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-Methoxythiophene | HCID 85610 | 76% |
| 생성물 | Sodium Methoxide | HCID 10942334 | — |
반응 단계
2-Methoxythiophene was prepared by the procedures described in H. A. Keeystra et aL, Tetrahedron, 1992, 48, 3633. Thus, a solution of sodium methoxide in methanol was prepared by adding sodium (2.12 g, 92.2 mmol) to methanol (14 ml). 2-Bromothiophene (10 g, 61.3 mmol) was added while maintaining reflux. Cuprous bromide (0.88 g, 6.1 mmol) was added and the mixture was maintained at reflux for 5.5 hours. A solution of sodium cyanide (3 g, 61.3 mmol) in water (30 ml) was added at 20-25° C. under vigorous stirring. The mixture was stirred until all solids dissolved, extracted with hexane, dried (Na2SO4), and concentrated to dryness. Distillation (90° C., 80 mm Hg) gave 2-methoxythiophene (5.35 g, 76%) as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06184242B2 |
| 출처 데이터셋 | uspto-grants-2001_02 |
| ORD ID | ord-e68399a59e98448abfbcb05e435ff2fd |
| 출처 메모 | uspto-grants-2001_02 |