Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Aluminium lithium hydride → 3-(2-Hydroxyethyl)-7-methoxybenzofuran
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 반응물 | Ethyl(7-methoxy-1-benzofuran-3-yl)acetate | HCID 22734085 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(2-Hydroxyethyl)-7-methoxybenzofuran | HCID 22662935 | — |
반응 단계
To a stirred suspension of LiAlH4 (200 mg, excess) in THF at 0° C., ethyl(7-methoxy-1-benzofuran-3-yl)acetate (1.17 g, 5 mmol) in THF (20 mL) was added slowly. After the addition, the reaction mixture was stirred at room temperature for 1 hr and quenched with saturated NH4Cl solution. The product was extracted with chloroform and washed well with water. It was dried over anhydrous MgSO4; filtered and concentrated. The product, 2-(7-methoxy-1-benzofuran-3-yl)ethanol obtained as a white oil, was pure enough and taken to the next step without purification. Yield: 800 mg (83%); 193 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07235569B2 |
| 출처 데이터셋 | uspto-grants-2007_06 |
| ORD ID | ord-d83110f8642d4bdfa4612a82f91eea31 |
| 출처 메모 | uspto-grants-2007_06 |