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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591620Generated: October 31, 2026

Diisobutylaluminum hydride → N-(1-(4-(hydroxymethyl)phenyl)piperidin-4-yl)benzamide

https://huagongshe.com/reaction/591620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantEthyl 4-(4-benzamidopiperidin-1-yl)benzoateHCID 66670912—
SolventTetrahydrofuranHCID 8028—
ProductN-(1-(4-(hydroxymethyl)phenyl)piperidin-4-yl)benzamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238640B2
Source datasetuspto-grants-2016_01
ORD IDord-82448bb50de94a589e8dc9c42f65ce2f
Source noteuspto-grants-2016_01