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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591609Generated: October 30, 2026

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

https://huagongshe.com/reaction/591609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantEthyl 4-(4-acetamidopiperidin-1-yl)benzoateHCID 66670978—
SolventDichloromethaneHCID 6344—
ProductN-(1-(4-(hydroxymethyl)phenyl)piperidin-4-yl)acetamideHCID 6674502624%

Reaction Steps

A solution of ethyl 4-(4-acetamidopiperidin-1-yl)benzoate (0.123 g, 0.42 mmol) in CH2Cl2 (10 mL) under nitrogen at −78° C. was treated with DIBAL-H (1.0M in hexanes, 0.950 mL, 0.95 mmol) dropwise, via a syringe. After 20 minutes, the mixture was warmed to room temperature, stirred for 1 hour, and quenched with 10% Rochelle's salt. After stirring for 10 minutes, CH2Cl2 (50 mL) was added, and the stirring was continued for 15 additional minutes. The layers were separated and the aqueous phase was extracted with CH2Cl2 (50 mL) and ethyl acetate (50 mL). The combined organic phases were dried (MgSO4), filtered, concentrated, and purified by flash chromatography on silica gel, eluting with 100% ethyl acetate to 10% MeOH/ethyl acetate to afford N-(1-(4-(hydroxymethyl)phenyl)piperidin-4-yl)acetamide as a white solid (0.025 g, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238640B2
Source datasetuspto-grants-2016_01
ORD IDord-a560f34ba5584bc1ac49f83144a939f1
Source noteuspto-grants-2016_01