Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tributylphosphine → (E)-3-(2,3-dihydro-benzo[1,4]dioxin-2-ylmethoxy)-but-2-enoic acid ethyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tributylphosphine | HCID 13831 | — |
| 반응물 | 1,4-Benzodioxane-2-methanol | HCID 19314 | — |
| 반응물 | Ethyl 2-butynoate | HCID 78043 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (E)-3-(2,3-dihydro-benzo[1,4]dioxin-2-ylmethoxy)-but-2-enoic acid ethyl ester | HCID 66899651 | 40.2% |
반응 단계
To a stirred mixture of (2,3-dihydro-benzo[1,4]dioxin-2-yl)-methanol (1.01 g, 5.90 mmol) and ethyl-2-butynoate (820 mg, 7.08 mmol) in tetrahydrofuran (15 mL) was added tri-n-butylphosphine (0.25 g, 1.18 mmol). The mixture was stirred at room temperature for 1.5 h. Upon completion of the reaction the tetrahydrofuran was removed in vacuo. The crude product obtained was purified by ISCO flash chromatography (Teledyne Isco RediSep Flash Column 40 g; 0% to 50% ethyl acetate/hexanes) to afford (E)-3-(2,3-dihydro-benzo[1,4]dioxin-2-ylmethoxy)-but-2-enoic acid ethyl ester (660 mg, 40%) as a colorless oil: LR-ES-MS m/z calculated for C15H18O5 [M]+ 278, observed [M+H]+ 279.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07741327B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-424f5c5691384160a9ed055e17cf6b2b |
| 출처 메모 | uspto-grants-2010_06 |