HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium sodium tartarate → (2-(Benzyloxy)-5-iodophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | 2-(Benzyloxy)-5-iodobenzaldehyde | HCID 15043489 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-(Benzyloxy)-5-iodophenyl)methanol | HCID 59831381 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
100 ml of a 1M diisobutylaluminum hydride solution in dichloromethane are added to a solution, cooled to 0° C., of 33.98 g (100.5 mmol) of 2-benzyloxy-5-iodobenzaldehyde (Example 2A) in 200 ml of dichloromethane. After stirring at 0° C. for 2 h, a saturated potassium sodium tartrate solution is added while cooling (highly exothermic reaction), and the reaction mixture is stirred for a further 2 h. After the separation of the phases, the organic phase is washed twice with water and once with a saturated aqueous sodium chloride solution and dried over sodium sulfate. The solvent is evaporated in vacuo. 31.8 g (93% of theory) of product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07446102B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-7bcd6824560e4b9c9644522f7863956a |
| Source note | uspto-grants-2008_11 |