HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530955Generated: October 30, 2026
3-Acetamidopiperidine → HCID 131735651, compound
https://huagongshe.com/reaction/530955
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Acetamidopiperidine | HCID 4169719 | — |
| Reactant | HCID 7175791 | HCID 7175791 | — |
| Reactant | HCID 12362975 | HCID 12362975 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131735651 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353114B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-6e45b9d26e444187a3c8d80cfad13703 |
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| Source note | uspto-grants-2016_05 |
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