HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 18448422, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18448416 | HCID 18448416 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18448422 | HCID 18448422 | 92.5% |
Reaction Steps
To solution of N-(2,4′-dimethyl-1,1′-biphenyl-3-yl)butanamide (15 g, 0.056 mol) in anhydrous tetrahydrofuran (500 ml) was added dropwise lithiumaluminium hydride (1 M solution in ether; 112 ml) under nitrogen. The resultant mixture was heated at 75° C. for 5.5 h then allowed to cool to room temperature for 16 h. To the reaction mixture was added dropwise wet ether (50 ml), then 2M NaOH (50 ml) and water (50 ml). The mixture was filtered, the solid residues washed with ether and the filtrate dried (Na2SO4), and the solvents removed in vacuo. The residue was partitioned between CH2Cl2 (400 ml) and water (20 ml). The CH2Cl2 layer was dried (Na2SO4) and the solvent removed in vacuo to afford the title compound as a yellow oil (13.12 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199239B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-c5c621b81ef3435491a1228e568c336b |
| Source note | uspto-grants-2007_04 |