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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492850Generated: October 30, 2026

Sodium Carbonate → 1-benzyl-N,N-dimethylpiperidin-4-amine dihydrochloride

https://huagongshe.com/reaction/492850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantDimethylamine, hydrochlorideHCID 10473—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Solvent1,1-DichloroethaneHCID 6365—
Product1-benzyl-N,N-dimethylpiperidin-4-amine dihydrochlorideHCID 23153393—

Reaction Steps

After adding 1-benzyl-4-piperidone (20 ml) and acetic acid (6.15 ml) to a suspension of dimethylamine hydrochloride (11.0 g) in dichloroethane (300 ml), the mixture was stirred in an ice bath. Sodium triacetoxyborohydride (34.3 g) was added thereto, and after stirring in an ice bath for 20 minutes, the mixture was further stirred for 5.5 hours at room temperature. Water (200 ml) was then added to the reaction mixture. Sodium carbonate was further added thereto until the aqueous layer became weakly alkaline, and the mixture was stirred for 10 minutes at room temperature. It was then partitioned and the aqueous layer was extracted with ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate. The dried organic layer was concentrated under reduced pressure. Diethyl ether (100 ml) and a 4N hydrochloric acid-ethyl acetate solution (59.5 ml) were added to the residue. This was diluted with diethyl ether (50 ml) and hexane (50 ml), and then the solid was filtered. The filtered solid was washed with diethyl ether. It was then subjected to aeration drying to provide a crude product of the title compound (30.0 g) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-73ada3998da94e71973f64fa7375b7cf
Source noteuspto-grants-2009_05