HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 21466310, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 15853103 | HCID 15853103 | — |
| Reactant | HCID 21466203 | HCID 21466203 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21466310 | HCID 21466310 | 32.8% |
Reaction Steps
To a solution prepared by dissolving 0.55 g of 2-trifluoromethyl-4-(4-ethoxyphenoxy)phenol, 0.40 g of 3,3-dibromoallyl alcohol and 0.49 g of triphenylphosphine in 10 ml of tetrahydrofuran, a solution prepared by dissolving 0.38 g of diisopropylazodicarboxylate in 5 ml of tetrahydrofuran was added dropwise at room temperature with stirring. After stirring at room temperature for 12 hours, the reaction solution was concentrated. Then, 20 ml of diethyl ether was added thereto, and the precipitate was filtered off. The resulting filtrate was concentrated, and subjected to silica gel column chromatography to give 0.30 g of 2-trifluoromethyl-4-(4-ethoxyphenoxy)-1-(3,3-dibromo-2-propenyloxy)benzene, yield 32%; nD24.0 1.5480.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05530015 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-6827ffe57f97477a86c5bb36550099f2 |
| Source note | uspto-grants-1996_06 |