HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → 1-[4-Chloro-2-benzoylphenyl]-3-phthalimidopropyne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-prop-2-ynylphthalimide | HCID 81644 | — |
| Reactant | 5-Chloro-2-iodobenzophenone | HCID 12948262 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[4-Chloro-2-benzoylphenyl]-3-phthalimidopropyne | HCID 12878252 | — |
Reaction Steps
A mixture of 0.71 g (4.0 mmole) of palladium chloride, 2.1 g (8.0 mmole) of triphenylphosphine, 0.80 g (4.2 mmole) of cuprous iodide, 68.8 g (0.20 mole) of 5-chloro-2-iodobenzophenone, 200 ml of diethylamine, and 400 ml of methylene chloride was stirred at room temperature under argon until complete solution was obtained. In one portion, 40.0 g (0.22 mole) of N-propargylphthalimide was added to the solution and the resulting mixture stirred for 20 hr. The volatiles were removed at reduced pressure and the residue was triturated with 200 ml of iospropanol. The resulting precipitate was collected by filtration to give crude end product. Recrystallization from acetone gave cream colored prisms, mp 148°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04259503 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-48a9bbd706104548b506c02d8a39b732 |
| Source note | uspto-grants-1981_03 |