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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846618Generated: November 3, 2026

Ammonium Chloride → tert-Butyl 4-(1-hydroxyethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1846618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Acetyl-piperidine-1-carboxylic acid tert-butyl esterHCID 10987983—
SolventEthanolHCID 702—
Producttert-Butyl 4-(1-hydroxyethyl)piperidine-1-carboxylateHCID 2198990396.6%

Reaction Steps

To a solution of 0.400 g (1.76 mmol) of 4-acetyl-piperidine-1-carboxylic acid tert-butyl ester in ethanol (3 mL) is added 0.134 g (3.52 mmol) of sodium borohydride. The mixture is stirred at room temperature for 1 hour then a saturated aqueous solution of ammonium chloride is added to consume excess reactants. The mixture is washed with ethyl acetate and the combined organic phase is dried over anhydrous sodium sulfate and concentrated under reduced pressure to provide 0.390 g (96.6%) of 4-(1-hydroxy-ethyl)-piperidine-1-carboxylic acid tert-butyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952004B2
Source datasetuspto-grants-2015_02
ORD IDord-a8f3e6c1c76f4cb0b106e7c11f4099d4
Source noteuspto-grants-2015_02