HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → (2-Iodoethyl)cyclohexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | (2-Bromoethyl)cyclohexane | HCID 15440 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (2-Iodoethyl)cyclohexane | HCID 12923931 | 85.1% |
Reaction Steps
Dissolve (2-bromo-ethyl)-cyclohexane (10.0 g, 52.3 mmol) in 500 mL acetone, add sodium iodide (15.6 g, 104.6 mmol) and reflux over night. Filter the reaction mixture, add water to the filtrate and extract with hexane. Dry the organic phases over sodium sulfate, filter and concentrate to an oil. Further purify this material by distillation to afford the title compound (10.6 g). 1H-NMR (CDCl3) δ=0.83-1.00 (m, 2H), 1.07-1.48 (m, 4H), 1.61-1.80 (m, 7H), 3.16-3.27 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576108B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-e9766b19f5fb475ea8c723f0880d395b |
| Source note | uspto-grants-2009_08 |