HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58893Generated: October 29, 2026
Water → Benzyl 2-(4-hydroxypiperidin-1-yl)acetate
https://huagongshe.com/reaction/58893
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 2-(4-hydroxypiperidin-1-yl)acetate | HCID 21805034 | 51% |
Reaction Steps
To piperidin-4-ol (HCl salt, 9.0 g) was added a solution of benzyl 2-bromoacetate (15.0 g, 65.7 mmol) in dichloromethane (100 mL). The mixture was cooled to 0° C. and triethylamine (27.6 mL, 0.200 mol) was added. The reaction mixture was allowed to warm to ambient temperature and stirred for 2 h. Water (100 mL) was added and the resulting mixture was extracted with dichloromethane (100 mL×3). The organic extracts were combined, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by flash column chromatography on silica gel (dichloromethane/methanol=20:1 to 10:1) to afford benzyl 2-(4-hydroxypiperidin-1-yl)acetate (8.3 g, 51% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434761B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-ec3130047fd144068202289247756349 |
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| Source note | uspto-grants-2016_09 |
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