HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalimide → 2-[3-(4-Trifluoromethylphenyl)-2-propenyl]phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 3-[4-(Trifluoromethyl)phenyl]prop-2-en-1-ol | HCID 53925727 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[3-(4-Trifluoromethylphenyl)-2-propenyl]phthalimide | HCID 69480736 | 93% |
Reaction Steps
4-(Trifluoromethyl)cinnamyl alcohol (3 g, 14.84 mmol) was dissolved in THF (60 ml), and phthalimide (2.84 g, 19.29 mmol) and triphenylphosphine (5.84 g, 22.26 mmol) were added to the solution, to which a solution of diethyl azodicarboxylate (3.87 g, 22.26 mmol) in THF (20 ml) was gradually added dropwise. The mixture was stirred at room temperature for 3 hours. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane/methylene chloride=1/1) to afford 2-[3-(4-trifluoromethylphenyl)-2-propenyl]phthalimide (4.57 g, yield 93%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07262212B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-938b1a119cb44be6a67436d808d3c453 |
| Source note | uspto-grants-2007_08 |