Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Boron trifluoride etherate → 4-Hydroxy-3-(1-(1-naphthyl)-propyl)-coumarin
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Boron trifluoride etherate | HCID 8000 | — |
| 반응물 | 1-(1-Naphthyl)-1-propanol | HCID 12453335 | — |
| 반응물 | 4-Hydroxycoumarin | HCID 54682930 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 4-Hydroxy-3-(1-(1-naphthyl)-propyl)-coumarin | HCID 54711575 | 51% |
반응 단계
To a cloudy solution of 324 mg of 4-hydroxycoumarin and 373 mg of 1-(1-naphthyl)-propan-1-ol of Preparation 22 in 7 mL of dioxane under an argon atmosphere is added 0.85 mL of boron trifluoride etherate. After stirring overnight the resulting yellow solution is concentrated under reduced pressure. The residue is partioned between water and ethyl acetate; the organic phase is washed with brine, dried (magnesium sulfate), and concentrated. The residue is adsorbed onto silica gel and then flashed column chromatographed using 40% to 50% ethyl acetate in hexane to yield 337 mg of the title product as a pale yellow solid. An analytical sample may be prepared by crystallization from ethyl acetate-hexanes.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05686486 |
| 출처 데이터셋 | uspto-grants-1997_11 |
| ORD ID | ord-2c5a7267544148f3b60aa14a06517759 |
| 출처 메모 | uspto-grants-1997_11 |