Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | 3-Oxotetrahydrofuran | HCID 529392 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68772367 | HCID 68772367 | 20.2% |
Reaction Steps
To a solution of dihydrofuran-3(2H)-one (0.5 g, 6.0 mmol, Small Molecules Inc.) in acetonitrile (10 mL) were added molecular sieves (0.5 g) and butan-1-amine (0.4 g, 5.5 mmol, Aldrich). The reaction mixture was stirred at room temperature overnight and then filtered. To the filtrate was added potassium thiocyanate (0.7 g, 7.3 mmol, Aldrich). The temperature was adjusted to 50° C. and the mixture was stirred until the solids were dissolved. Then, iodine (2.8 g, 10.9 mmol, EMD Chemicals) was added to the mixture and stirred at 50° C. overnight. The reaction mixture was cooled, concentrated and dissolved in EtOAc (15 mL). The solution was washed with Na-meta-bisulfite 20% (15 mL) by mixing the layers for 30 minutes. The organic layer was washed twice with 1N HCl (15 mL). The aqueous layers (metabisulfite and HCl) were combined and the pH was adjusted to pH ˜9 by adding NH4OH. The product was extracted with EtOAc (4×20 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated to obtain the crude product (0.22 g) of the title compound. MS (ESI+) m/z 199 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08735434B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-180b65222ca44fa8a28cb8a7916dee97 |
|---|
| Source note | uspto-grants-2014_05 |
|---|