HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylaluminum hydride → N-(1-(4-(hydroxymethyl)phenyl)piperidin-4-yl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Ethyl 4-(4-benzamidopiperidin-1-yl)benzoate | HCID 66670912 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(1-(4-(hydroxymethyl)phenyl)piperidin-4-yl)benzamide | HCID 66745757 | — |
Reaction Steps
A solution of ethyl 4-(4-benzamidopiperidin-1-yl)benzoate (4.2 g, 11.9 mmol) in THF (400 mL) was cooled to 0° C. under nitrogen and treated with DIBAL-H (1.0 M in THF, 47 mL, 47 mmol). The mixture was warmed to room temperature and stirred for 1 hour. Then, the reaction mixture was quenched with Rochelle's salt (10% aqueous), concentrated to remove the THF, brine (300 mL) was added, and the organic phase was extracted with CH2Cl2 (3×200 mL), dried over anhydrous MgSO4, filtered, and concentrated, to afford N-(1-(4-(hydroxymethyl)phenyl)piperidin-4-yl)benzamide as a yellow solid that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238640B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-82448bb50de94a589e8dc9c42f65ce2f |
| Source note | uspto-grants-2016_01 |