HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 11-Bromoundecylmaleimide pentacene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 11-Bromo-1-undecanol | HCID 74163 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | Pentacene maleimide | HCID 86643198 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 11-Bromoundecylmaleimide pentacene | HCID 86647752 | — |
| Product | N-(11-bromoundecyl) maleimide pentacene | HCID 86647754 | — |
Reaction Steps
Pentacene-maleimide adduct (5c) (375 mg, 1 mmole) are added to a solution of triphenyl phosphine (393 mg, 1.5 mmole) and 11-bromo-1-undecanol (375 mg, 1.5 mmole) in 40 mL of anhydrous tetrahydrofuran. To this mixture a solution of diisopropyl azodicarboxylate (300 mg, 1.5 mmole) in 10 mL of anhydrous THF is added dropwise under a stream of nitrogen. After completion of the addition, the solution is stirred at room temperature for 18 hours. The solvent is evaporated under reduced pressure and the residue is titrated with diethyl ether and the precipitate is filtered, washed with 1:1 ether-hexane and dried. Crystallization from benzene affords the pure sample of 11-bromoundecylmaleimide-pentacene adduct 5d.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07771695B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-8ca79133d16f4ad49136e6255d18ca23 |
| Source note | uspto-grants-2010_08 |