HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodide Ion → 6-iodo-2,3-dihydro-1H-inden-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | Indan-5-amine | HCID 90496 | — |
| Catalyst | HCID 178418844 | HCID 178418844 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-iodo-2,3-dihydro-1H-inden-5-amine | HCID 22400293 | — |
Reaction Steps
A mixture of 5-aminoindan (423 mg, 3.17 mmol), silver sulfate (990 mg, 3.17 mmol) and iodide (805 mg, 3.17 mmol) in CH3OH (20 mL) was stirred at room temperature overnight. The mixture was filtered and the solid was washed with a small amount of CH3OH. The filtrate was quenched with saturated Na2S2O3 and then diluted with water. The aqueous layer was extracted with EtOAc (3×). The combined organic layers were washed with brine (1×), dried (Na2SO4) and concentrated in vacuo. Flash chromatography (Si, hexanes/EtOAc) of the residue afforded 6-iodoindan-5-amine. LCMS calc.=260.0; found=260.0 (M+1)+. 1H NMR (500 MHz, CDCl3) δ 7.51 (s, 1H), 6.69 (s, 1H), 3.97 (br, s, 2H), 3.02-2.90 (m, 1H), 2.81 (d, J=7.1 Hz, 3H), 2.12-2.02 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910592B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-136a2d2a1a8645b680e7a34a2069da15 |
| Source note | uspto-grants-2011_03 |