HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylaluminumhydride → HCID 68510790, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 68507568 | HCID 68507568 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68510790 | HCID 68510790 | — |
Reaction Steps
To a solution of 2-ethoxy-4′-fluoro-biphenyl-4-carboxylic acid ethyl ester (0.50 g, 1.73 mmol, 1.0 equiv) in anhydrous THF (10 mL) was added dropwise at −10° C. diisobutylaluminum hydride (5.2 mL, 5.20 mmol, 3.0 equiv; 1 M solution in hexane) and the ccolong bath removed. After stirring for an additional time period of 60 min at rt, the reaction mixture was carefully poured on crashed ice/diluted HCl, extracted twice with ethyl acetate, the combined organic phases washed with water and a sat. solution of NaCl, dried over MgSO4 and concentrated by evaporation under reduced pressure. The title compound was isolated in quantitative yield (0.43 g) as a colorless viscous oil, sufficiently pure for the next step. MS (ISP): 229.3 [M+H−H2O]1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07799806B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-c04050c6a2284c0d8f132fe59b8dff13 |
| Source note | uspto-grants-2010_09 |