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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530955Generated: October 30, 2026

3-Acetamidopiperidine → HCID 131735651, compound

https://huagongshe.com/reaction/530955

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AcetamidopiperidineHCID 4169719—
ReactantHCID 7175791HCID 7175791—
ReactantHCID 12362975HCID 12362975—
SolventMethanolHCID 887—
ProductHCID 131735651HCID 131735651—

Reaction Steps

(c)Preparation of (R)—N-piperidin-3-ylacetamide Dibenzyol tartarate salt: In a RBF charged 500 ml of Methanol, 50 gm of N-piperidin-3-ylacetamide & 138 gm of L (+)-Dibenzoyl tartaric acid. The reaction was maintained for about 90 mins at room temperature and then heated to reflux. The reaction mass was maintained for about an hour at reflux and then cooled and maintained at room temperature for about 12.0 hours. Then, the product was filtered and washed with 100 ml methanol. Again charged the obtained wet cake in 800 ml methanol, heated to reflux and maintained reaction mass for 1.0 hr to get a clear solution. Cooled the reaction mass to room temperature and maintained for 12.0 hrs. The product was filtered and washed with 100 ml methanol. The product was dried at about 45-50° C. under vacuum. Unwanted S-isomer NMT 1.5% Dry Wt-20. Gm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353114B2
Source datasetuspto-grants-2016_05
ORD IDord-6e45b9d26e444187a3c8d80cfad13703
Source noteuspto-grants-2016_05