HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl Alcohol → HCID 58080850, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | HCID 58080843 | HCID 58080843 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58080850 | HCID 58080850 | — |
Reaction Steps
0.4 mL of allyl alcohol and 1.5 mL of diisopropyl azodicarboxylate were added dropwise at room temperature in an argon atmosphere to a solution containing 1 g of the compound obtained in Step 2 and 2 g of triphenylphosphine dissolved in 100 mL of tetrahydrofuran, and then reacted for 16 hours. The reaction solution was diluted with water, followed by extraction with ethyl acetate (100 mL×2). Then, the extract was dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated, and the obtained crude product was purified by silica gel column chromatography (acetone:hexane=1:2) to obtain 550 mg of the compound of interest as a colorless oil (50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08951997B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-9e427d44ce394ac78fd526e4375cb523 |
| Source note | uspto-grants-2015_02 |