HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → {2-Chloro-6-[(diethylamino)methyl]phenyl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 2-chloro-6-[(diethylamino)methyl]benzoate | HCID 59589357 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {2-Chloro-6-[(diethylamino)methyl]phenyl}methanol | HCID 59589378 | 85% |
Reaction Steps
To methyl 2-chloro-6-[(diethylamino)methyl]benzoate (3.97 g, 15.5 mmol) in anhydrous THF (100 mL) was added a solution of diisobutylaluminium hydride (1 M in toluene, 35 mL, 35 mmol). The reaction mixture was stirred at room temperature for 90 minutes. A Rochelle's salt solution (200 mL) and dichloromethane (200 mL) were added. The mixture was stirred at room temperature for 2 hours. The organic layer was recovered, dried over MgSO4, filtered, evaporated, and dried in vacuo, affording {2-chloro-6-[(diethylamino)methyl]phenyl}methanol (3.0 mg, 85% yield), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315521B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-473e18fb81314d38a2172f61f8768b67 |
| Source note | uspto-grants-2016_04 |