Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → Methyl 2-(6-hydroxy-1-benzofuran-3-yl)acetate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester | HCID 17453 | — |
| 반응물 | 6-Hydroxy-3-coumaranone | HCID 235717 | — |
| 생성물 | Methyl 2-(6-hydroxy-1-benzofuran-3-yl)acetate | HCID 20770861 | — |
반응 단계
A mixture of 6-hydroxy-(2H)-benzofuran-3-one (5.0 g, 33.3 mmol), methyl (triphenylphosphoranylidene)acetate (25.0 g, 73 mmol), and xylenes (100 mL) is refluxed 6 hr. The reaction is concentrated and diluted with enough 1M aqueous hydrochloric acid to adjust pH to 2-3. The product is extracted into ethyl acetate (3×100 mL). The combined extracts are dried over anhydrous magnesium sulfate, filtered and concentrated. The residue is purified via silica chromatography eluting with 7:3 hexanes:ethyl acetate to afford the product as a orange oil, 1.3 g, 20%. MS M++1 207. The structure is confirmed by 1H NMR spectroscopy.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07528160B2 |
| 출처 데이터셋 | uspto-grants-2009_05 |
| ORD ID | ord-2e9f6240f632462d98765b5979e85e6b |
| 출처 메모 | uspto-grants-2009_05 |