HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoamyl Nitrite → 6-Iodoindane-5-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | 6-amino-2,3-dihydro-1H-indene-5-carbonitrile | HCID 45122176 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-Iodoindane-5-carbonitrile | HCID 57576269 | — |
Reaction Steps
A mixture of 6-aminoindane-5-carbonitrile (48.5 mg, 0.307 mmol), isoamyl nitrite (82 μL, 0.614 mmol) and iodide (85.7 mg, 0.338 mmol) in dry CHCl3 (2 mL) was stirred at room temperature for 0.5 h. The mixture was then heated at 80° C. under N2 for 2 h. The reaction mixture was quenched with saturated Na2S2O3 and partitioned between CH2Cl2 and water. The organic layer was dried (Na2SO4) and concentrated in vacuo. The residue was purified by flash chromatography (Si, 1% EtOAc in hexanes) to afford 6-iodoindane-5-carbonitrile. LCMS calc.=270.0; found=270.0 (M+1)+. 1H NMR (500 MHz, CDCl3) δ 7.78 (s, 1H), 7.48 (s, 1H), 2.96 (t, J=7.5 Hz, 2H), 2.92 (t, J=7.5 Hz, 2H), 2.16-2.10 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910592B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-db9018ef49c042158934b1e46d0db72c |
| Source note | uspto-grants-2011_03 |