HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylaluminumhydride → HCID 21023777, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 86590568 | HCID 86590568 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21023777 | HCID 21023777 | 99% |
Reaction Steps
To a cooled (−78° C.) solution of 4-cyclohexyl-4-(2-methoxy-carbonylethyl)-piperidine-1-carboxylic acid tert-butyl ester, 9, (1.0 g, 2.833 mmol) in 40 ml of anhydrous methylene chloride is added diisobutylaluminum hydride (5.75 ml, 1 M, 5.75 mmol). The reaction is stirred at room temperature for 40 min before it is quenched by adding methanol (3 mL) and water (20 mL). The reaction mixture is warmed to room temperature and the organic layer separated, dried over sodium sulfate, filtered and concentrated in vacuo to afford 915 mg (>99% yield) of the desired compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07026335B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-d594b9b91b6a4183a02728c06c55ebfa |
| Source note | uspto-grants-2006_04 |