참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Propargyl bromide | HCID 7842 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Methyl 3-hydroxy-2-naphthoate | HCID 70163 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Methyl-3-propargyloxy-2-naphthoate | HCID 54262446 | 35% |
반응 단계
Methyl-3-hydroxy-2-naphthoate (2.63 g, 0.013 mol) was dissolved in dry THF (80 ml) and treated with sodium hydride (80%) ((0.398 g, 0.013 mol), with stirring under N2. After 0.5 h, propargyl bromide (80% in toluene) (2.57 ml 0.017 mol) was added and the mixture heated to reflux. After 20 h, the reaction mixture was allowed to cool and then evaporated under reduced pressure. The residue was then evaporated under reduced pressure. The residue was then partitioned between EtOAc and water. The aqueous layer was then extracted with EtOAc (1×), and the combined organic layers were dried (Na2SO4) and evaporated to given an orange oil. Crystallisation of the oil from petrol (60/80) diethyl ether provided the title compound as a pale yellow solid (1.0 gg, 35%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05726187 |
|---|
| 출처 데이터셋 | uspto-grants-1998_03 |
|---|
| ORD ID | ord-33fdd502bd9b4b6ab4abded4f14a5ab2 |
|---|
| 출처 메모 | uspto-grants-1998_03 |
|---|