HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isocyanate → HCID 68839001, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 68839387 | HCID 68839387 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68839001 | HCID 68839001 | — |
Reaction Steps
Tetrabutylammonium fluoride (1.0M in THF, 2 mL) is added to a solution of PS-isocyanate resin (0.5 g) in THF (2 mL) and the mixture is stirred at RT for 2 h. The resin is filtered off and the filtrate is added to a solution of 5-[2-benzyloxy-4-((E)-3-phenylpropenyl)-phenyl]-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-one (89 mg, 0.163 mmol) in THF (1 mL). The reaction is stirred at 75° C. for 1 h then the mixture is cooled and concentrated. The residue is partitioned between EtOAc and water and the organic layer is washed with 2N HCl (3×) and brine. The organic layer is dried over sodium sulfate and the solvent removed under reduced pressure to afford the title compound as a light yellow foam: (M−1)−=433.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084448B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-d6a893671b964c8e8ec87126ee0a061b |
| Source note | uspto-grants-2011_12 |