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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantBenzyl bromoacetateHCID 62576—
ReactantPiperidin-4-olHCID 79341—
SolventDichloromethaneHCID 6344—
ProductBenzyl 2-(4-hydroxypiperidin-1-yl)acetateHCID 2180503451%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434761B2
Source datasetuspto-grants-2016_09
ORD IDord-ec3130047fd144068202289247756349
Source noteuspto-grants-2016_09