HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Biphenyl-4-yl 3-phenoxyacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Piperidinemethanol | HCID 420771 | — |
| Reactant | HCID 131736279 | HCID 131736279 | — |
| Product | Biphenyl-4-yl 3-phenoxyacrylate | HCID 131736282 | — |
Reaction Steps
4-Piperidinemethanol (0.06 g, 0.5 mmol) and compound 3 (0.11 g, 0.5 mmol) [4 (0.22 g, 0.5 mmol) or 5 (0.19 g, 0.5 mmol)] were dissolved in dry THF (5 mL), and the solution was stirred at room temperature for 30-45 min. The solvent was removed under reduced pressure at room temp to give the crude product which was then purified by column chromatography using ethyl acetate:hexane (7:3 or 8:3) to give compound 6 (7 or 8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09393306B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-d727b0a42c7845fc9670aa664388b319 |
| Source note | uspto-grants-2016_07 |