HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 2-(Iodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-(Bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 10955110 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(Iodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 10901594 | 98.9% |
Reaction Steps
To the mixture of 2-(bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2.0 g, 8.3 mmol) synthesized in Production Example 2 and acetone (17 ml), sodium iodide (1.9 g, 13 mmol) was added at room temperature, and the obtained reaction mixture was stirred at room temperature for 2 hours. Impurities were removed by filtration, and the solvents were evaporated under reduced pressure from the filtrate. Hexane was added to the obtained residue, and insoluble matter was removed by filtration. The solvents were evaporated under reduced pressure from the filtrate, thereby obtaining the entitled compound (2.2 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273885B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-a063da5f07224eab8d34d60cc280de6a |
| Source note | uspto-grants-2012_09 |