HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 2-(2-(2-Iodoethoxy)ethoxy)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-(2-(2-Chloroethoxy)ethoxy)ethanol | HCID 78871 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(2-(2-Iodoethoxy)ethoxy)ethanol | HCID 14765039 | 80.8% |
Reaction Steps
A 25 ml reaction flask, equipped with a reflux condenser, an oil bath and a magnetic stirrer was charged with 2 g (11.9 mmol) of 2-[2-(2-chloroethoxy)-ethoxy]-ethanol (Fluka), 4 g of sodium iodide and 3 g of sodium hydrogencarbonate in 20 ml of Acetone. The reaction mixture is refluxed over night and when cold, filtered. The filtrate is concentrated at the rotavap, dissolved in 5 ml of CH2Cl2 and filtered again. Then the filtrate is concentrated again at the rotavap to yield 2.5 g of a yellow oil. The NMR shows a pure substance (CDCl3) 2.58 s broad (1H/OH); 3.22 t (2H/CH2-J); 3.53-3.77 m (10H/CH2—O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897779B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-33165b966d6b4ae18e589dde0532ab86 |
| Source note | uspto-grants-2011_03 |