HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 69673475, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-(3-Butynyl)phthalimide | HCID 11171619 | — |
| Reactant | 4-broMo-2-phenylthiazole | HCID 11831528 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 69673475 | HCID 69673475 | 55.6% |
Reaction Steps
To 221 mg of dichlorobis(triphenylphosphine)palladium, 60 mg of copper iodide, and 1.24 g of N-(3-butynyl)phthalimide were added 15 ml of tetrahydrofuran, 1.50 g of the 2-phenyl-4-bromothiazole obtained in the foregoing stage, and 3.8 ml of triethylamine in a nitrogen atmosphere, and the mixture was stirred under reflux for 4 hours. After the stifling, the reaction mixture was cooled to room temperature and the solids were filtered. After concentrating the filtrate, the residue was purified by column chromatography (Wakogel C-200; toluene:ethyl acetate=9:1) to give 1.24 g of a phthalimide compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09089139B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-3145085443a94fa186d80d27f3432910 |
| Source note | uspto-grants-2015_07 |